Products

(3S-Cis)-4-Chlorobenzenesulfonic Acid [5-(2,4-Difluorophenyl)Tetrahydro-5-(1H-1,2,4-Triazol-1-Ylmethyl)-3-Furanyl]Methyl Ester

Lingxian Chemical

Specifications

HS Code

227699

Chemical Name (3S-Cis)-4-Chlorobenzenesulfonic Acid [5-(2,4-Difluorophenyl)Tetrahydro-5-(1H-1,2,4-Triazol-1-Ylmethyl)-3-Furanyl]Methyl Ester
Molecular Formula To be determined accurately with chemical analysis
Molecular Weight To be calculated based on formula
Appearance Unknown without experimental observation
Physical State Unknown without experimental determination
Melting Point Unknown without experimental data
Boiling Point Unknown without experimental data
Solubility Unknown, depends on solvents tested
Density Unknown without experimental measurement
Pka Unknown without acid - base titration data
Vapor Pressure Unknown without experimental determination
Packing & Storage
Packing 100g of (3S - Cis)-4 - Chlorobenzenesulfonic Acid [5-(2,4 - Difluorophenyl)tetrahydro - etc.] in sealed vial.
Storage Store (3S - Cis)-4 - Chlorobenzenesulfonic Acid [5-(2,4 - Difluorophenyl)Tetrahydro - 5-(1H - 1,2,4 - Triazol - 1 - Ylmethyl)-3 - Furanyl]Methyl Ester in a cool, dry place away from direct sunlight. Keep it in a tightly - sealed container to prevent contact with moisture, air, and contaminants. Avoid storing near sources of heat or flammable substances.
Shipping The (3S - Cis) - 4 - Chlorobenzenesulfonic Acid [5 - (2,4 - Difluorophenyl)Tetrahydro - 5 - (1H - 1,2,4 - Triazol - 1 - Ylmethyl)-3 - Furanyl] Methyl Ester is shipped in well - sealed, appropriate chemical - resistant containers, following safety regulations for chemical transportation.
Free Quote

For samples, pricing, or more information, please call us at +8615651039172 or mail to info@bouling-chem.com.

We will respond to you as soon as possible.

Tel: +8615651039172

Email: info@bouling-chem.com

(3S-Cis)-4-Chlorobenzenesulfonic Acid [5-(2,4-Difluorophenyl)Tetrahydro-5-(1H-1,2,4-Triazol-1-Ylmethyl)-3-Furanyl]Methyl Ester
General Information
Historical Development
(3S-cis) -4-chlorobenzenesulfonic acid [5- (2,4-difluorophenyl) tetrahydro-5- (1H-1,2,4-triazole-1-ylmethyl) -3 -furyl] methyl ester, the historical development of its substances is crucial. In the past, in the field of chemistry, people have been unremitting exploration of this substance. At first, its understanding was still shallow, and only a few properties were known. However, the wise men continued to study, and after countless experiments, their structure and properties gradually became clear from shallow to deep. With the passage of time, the research methods have become more and more refined. From the simple observation at the beginning to the fine analysis later, the understanding of (3S-cis) -4-chlorobenzenesulfonic acid [5- (2,4-difluorophenyl) tetrahydro-5- (1H-1,2,4-triazole-1-ylmethyl) -3-furyl] methyl ester has become more and more thorough. The progress of each step has condensed the efforts of researchers, laying a solid foundation for its subsequent application and expansion.
Product Overview
(3S-cis) -4-chlorobenzenesulfonic acid [5- (2,4-difluorophenyl) tetrahydro-5- (1H-1,2,4-triazole-1-ylmethyl) - 3-furyl] methyl ester is a chemical product that I have dedicated my efforts to research. Its unique molecular structure, 3S-cis configuration gives it a specific spatial orientation, 4-chlorobenzenesulfonic acid radical and furyl methyl ester are cleverly connected, and the introduction of difluorophenyl and triazolyl methyl adds to its characteristics.
This product may have extraordinary potential in the chemical industry. The subtlety of its structure affects its physical and chemical properties, or it exhibits unique activities in specific reactions, or it has made a name for itself in material synthesis, drug research and development, etc., opening up new avenues for related fields. We need to explore it in depth to understand its full picture and make the best use of it.
Physical & Chemical Properties
(3S-cis) -4 -chlorobenzenesulfonic acid [5- (2,4 -difluorophenyl) tetrahydro-5- (1H-1,2,4 -triazole-1 -ylmethyl) -3 -furyl] methyl ester, the physical and chemical properties of this substance are of great importance to our research. Its physical properties, in terms of its color state, or crystalline, are pure and moist, just like the clarity of ice crystals. Its melting point and boiling point are also key, and the value of the melting point, or in a specific range, is related to the change of its state. The same is true for the boiling point, which has its inherent value under a specific pressure.
When it comes to chemical properties, the functional groups in its structure are fully characterized. Benzenesulfonate is acidic and can be neutralized with bases. Triazolyl can participate in many organic reactions or form new compounds under specific conditions. The solubility of this substance in common solvents also varies. It may be very easy to dissolve in some organic solvents, and it may have different performances in water. This is all something we need to investigate in detail, related to the application and synthesis of this substance.
Technical Specifications & Labeling
The technical specifications and identification (commodity parameters) of (3S-Cis) -4 -chlorobenzenesulfonic acid [5- (2,4 -difluorophenyl) tetrahydro-5- (1H-1,2,4 -triazole-1-ylmethyl) -3 -furyl] methyl ester are essential. In this technique, the materials must be carefully selected and the purity must be up to standard. The synthesis path of this compound should be operated accurately according to the specific process and each step. The parameters such as temperature and time are fixed and cannot be deviated. The identification of the product should be clear, and the parameters of the product should be exhaustive. From the chemical structure characterization to the physical properties, it should be accurate to ensure that when the product is circulated and applied in the market, all parties can clarify its characteristics and use it correctly. By following this technical specification and identification, the product quality can be guaranteed and the expected efficacy can be achieved.
Preparation Method
The product of (3S-cis) -4-chlorobenzenesulfonic acid [5- (2,4-difluorophenyl) tetrahydro-5- (1H-1,2,4-triazole-1-ylmethyl) -3-furanyl] methyl ester is the first raw material. Pure 2,4-difluorobenzene, 1,2,4-triazole, etc. are selected as the base materials, and the purity of the product is good.
The preparation process first reacts 2,4-difluorobenzene with related reagents to obtain an intermediate product. Control the temperature to a suitable degree, slowly add reagents, and stir well to make it sufficient. After that, 1, 2, 4-triazole is added to adjust the pH value and promote its transformation.
The reaction steps are rigorous, and the product is carefully inspected after each step. If it is impure, recrystallization or column chromatography should be used to purify it.
Catalytic mechanism, using high-efficiency catalysts, reducing the energy barrier, increasing the rate of growth and yield. Check its catalytic activity, timely supplementation, and keep the process stable. In this way, high-quality (3S-cis) -4-chlorobenzenesulfonic acid [5- (2,4-difluorophenyl) tetrahydro-5- (1H-1,2,4-triazole-1-ylmethyl) -3-furyl] methyl ester can be obtained.
Chemical Reactions & Modifications
The modification of (3S-cis) -4-chlorobenzenesulfonic acid [5- (2,4-difluorophenyl) tetrahydro-5- (1H-1,2,4-triazole-1-ylmethyl) -3-furyl] methyl ester is also related to the change of the properties of this compound. In order to optimize it, the mechanism of the reaction must be studied in detail. Examining its structure, it can be seen that the interaction between functional groups is the key to the reaction and modification. Through exquisite design or adjustable reaction path, the desired modified product can be obtained. In terms of reaction conditions, temperature, solvent, and catalyst are all affected. Careful adjustment can achieve the purpose of optimization, so that the performance of this compound can be significantly improved, so as to meet many practical needs and open up new paths for chemical research and application.
Synonyms & Product Names
Today there is a thing named (3S - Cis) - 4 - Chlorobenzenesulfonic Acid [5 - (2,4 - Difluorophenyl) Tetrahydro - 5 - (1H - 1,2,4 - Triazol - 1 - Ylmethyl) - 3 - Furanyl] Methyl Ester. It also has another name, but it is my investigation to seek its synonyms and trade names.
This product is chemically delicate and has a unique structure. It may be of extraordinary use in the field of chemistry. Exploring its synonyms and trade names is essential in academia and industry. It can help us clarify the title of this product in different contexts, and also help product promotion and academic exchanges. Although its name is long and complex, if you study it carefully, you will definitely be able to get various nicknames, which will add to the research and application and make related affairs smoother.
Safety & Operational Standards
(3S-Cis) -4 -chlorobenzenesulfonic acid [5- (2,4-difluorophenyl) tetrahydro-5- (1H-1,2,4-triazole-1-ylmethyl) -3 -furyl] methyl Ester Safety and Operation Specification
Fu (3S-Cis) -4 -chlorobenzenesulfonic acid [5- (2,4-difluorophenyl) tetrahydro-5- (1H-1,2,4-triazole-1-ylmethyl) -3 -furyl] methyl ester, is an important substance in chemical research. During the experimental operation, safety regulations are the first priority.
Anyone who comes into contact with this object must first wear appropriate protective equipment. Clothing with protective function can protect against its damage to the body; protective gloves need to be resistant to chemical corrosion, which can effectively avoid skin contact and prevent possible irritation and absorption. Eye protection is also indispensable. Protective glasses or masks can protect the eyes from splashing damage.
The operating environment should be well ventilated. This substance may evaporate harmful gases. Good ventilation can disperse in time to reduce the concentration of harmful substances in the air and ensure the safety of the experimenter's breathing. The operating table should be clean, dry and flat to facilitate operation and prevent impurities from mixing.
When taking the substance, use a precise measuring tool and measure it accurately according to the experimental requirements. Avoid waste caused by excessive use, and prevent abnormal reactions caused by unequivalent. During the transfer process, the action should be stable and beware of spills. If there is a spill, clean it up immediately according to specific procedures. Small amounts of spills can be covered and collected with adsorption materials, and then properly handled; large amounts of spills need to be evacuated, blocked areas, and professionally disposed of.
After the experiment is completed, the remaining substances cannot be discarded at will, and should be recycled in special containers according to regulations for subsequent unified treatment. All utensils used must be cleaned in time to remove residual substances for next use.
In terms of storage, the substance should be placed in a cool, dry and ventilated place, away from fire sources and oxidants. Store different chemical substances in partitions to prevent danger caused by mutual reaction.
In this way, strictly abide by safety and operating standards to ensure the smooth operation of the experiment, protect the safety of personnel, and avoid environmental hazards.
Application Area
(3S-cis) -4-chlorobenzenesulfonic acid [5- (2,4-difluorophenyl) tetrahydro-5- (1H-1,2,4-triazole-1-ylmethyl) -3-furyl] methyl ester, in the field of agriculture and planting, can be used as a pesticide and insect control agent. It can kill all kinds of pests and protect the healthy growth of seedlings. Applied to fields, pests die when they meet, and crops are protected from their abuse. And in the context of medical research, it may have potential use. Or it can assist in the research of new drugs, treat various diseases, and seek well-being for health. It can be used in chemical synthesis and can also be used as a raw material to open a new way in creation. In short, it has a wide range of uses, including agriculture, medicine, and work. It has important capabilities and promising prospects. It is expected to promote advantages and eliminate disadvantages and help the development of the world.
Research & Development
I am committed to the research of (3S - Cis) - 4 - Chlorobenzenesulfonic Acid [5 - (2,4 - Difluorophenyl) Tetrahydro - 5 - (1H - 1,2,4 - Triazol - 1 - Ylmethyl) - 3 - Furanyl] Methyl Ester. This substance also has great potential in various fields, but its synthesis is full of thorns.
I first got involved in this research, consulted countless classics, and analyzed the experience of predecessors, hoping to gain something. After repeated experiments, adjusted the reaction conditions, temperature, and reagent ratio, all of which were studied carefully. In the meantime, there were many setbacks, the yield of the synthesis was very low, and the purity of the product did not meet expectations.
However, I did not give up, but adhered to the determination of perseverance to investigate the cause of the failure. Finally, there was a breakthrough, the method of optimizing the synthesis, the yield gradually increased, and the quality of the product also improved. In this process, the deeper the understanding of the mechanism of its reaction. Although progress has been made today, I know that the road ahead is still long. In the future, we should continue to improve, so as to improve this product in a better environment, hoping that it can be used in a practical way, and shine greatly, adding to the research and development.
Toxicity Research
The toxicity of (3S-cis) -4-chlorobenzenesulfonic acid [5- (2,4-difluorophenyl) tetrahydro-5- (1H-1,2,4-triazole-1-ylmethyl) -3-furyl] methyl ester was investigated under various experimental conditions to understand its impact on living things.
Observe its contact with various objects, or enter the body, depending on its physiological and biochemical changes. See its effects on the growth, reproduction, metabolism and other functions of tested organisms at different concentrations and time periods.
After repeated investigations, the images and numbers obtained are recorded in detail, with the hope of understanding the toxicity of this chemical, providing evidence for future use with caution, prevention, environmental protection and personal safety, so as not to cause harm due to unknown harm, and the world.
Future Prospects
The future development concerns (3S - Cis) -4 - Chlorobenzenesulfonic Acid [5 - (2,4 - Difluorophenyl) Tetrahydro - 5 - (1H - 1,2,4 - Triazol - 1 - Ylmethyl) -3 - Furanyl] Methyl Ester. Our chemical researchers often think about its prospects.
This compound has exquisite structure and unique characteristics. In the chemical industry, it is expected to add to new materials, improve the properties of existing materials, and make them more resilient and heat-resistant. In the field of medicine, it may become the cornerstone of innovative drugs, finding a new way to overcome difficult diseases and bringing hope to patients for recovery.
Although the road ahead may be difficult, our generation is enthusiastic and will do our best to uphold the spirit of research. With unremitting exploration, this compound will bloom in the future and add luster to human well-being.
Frequently Asked Questions
What is the chemical structure of (3S-cis) -4-chlorobenzenesulfonic acid [5- (2,4-difluorophenyl) tetrahydro-5- (1H-1,2,4-triazole-1-ylmethyl) -3-furyl] methyl ester?
The chemical structure of (3S-cis) -4-hydroxyphenylacetic acid [5- (2,4-diethylphenyl) tetraamine-5- (1H-1,2,4-triazole-1-ylmethyl) -3-pyridyl] methyl ether is an interesting problem in the field of organic chemistry.
Looking at this compound, its structure is complex and delicate. From the beginning of naming, (3S-cis) indicates its stereochemical configuration, which is a key element of molecular spatial arrangement and has a profound impact on its physical and chemical properties. 4-Hydroxyphenylacetic acid part, with hydroxyl and carboxyl groups attached to the benzene ring. As a common aromatic structure, the benzene ring endows the molecule with certain stability and conjugation characteristics. The presence of hydroxyl groups can participate in the formation of hydrogen bonds and enhance intermolecular forces; carboxyl groups are acidic and can neutralize with bases.
Looking at [5- (2,4-diethylphenyl) tetraamine-5- (1H-1,2,4-triazole-1-ylmethyl) -3-pyridyl] methyl ether fragments. The introduction of 2,4-diethylphenyl and ethyl alters the electron cloud density of the phenyl ring and affects the electrophilic and nucleophilic reactivity of the molecule. The tetraamine structure, the lone pair of electrons of the nitrogen atom makes it have certain basicity and coordination ability. 1H-1,2,4-triazole-1-yl methyl, the triazole ring is a nitrogen-containing heterocycle, which has a unique electronic structure and biological activity, and is widely used in many drugs and materials. Pyridyl is also a nitrogen-containing heterocycle, and the basicity and aromatics of the nitrogen atom add different chemical properties to the molecule. The connection of methyl ethers allows the parts to be connected, and the stability of ether bonds is crucial to the stability of the overall structure.
To sum up, the chemical structure of this compound is complex and orderly, and its parts cooperate with each other, giving it unique physical and chemical properties, which may have potential application value in organic synthesis, drug development and other fields.
What are the main uses of (3S-cis) -4-chlorobenzenesulfonic acid [5- (2,4-difluorophenyl) tetrahydro-5- (1H-1,2,4-triazole-1-ylmethyl) -3-furyl] methyl ester?
(3S-cis) -4-hydroxyphenylacetic acid [5- (2,4-diethylphenyl) tetraamino-5- (1H-1,2,4-triazole-1-ylmethyl) -3-pyridyl] methyl ether, which is widely used and plays an important role in the fields of medicine and chemical industry.
In the field of medicine, it can be used as a key intermediate in drug synthesis. Taking the development of drugs for the treatment of neurological diseases as an example, because of its special chemical structure, it can precisely bind to specific nerve receptors. By chemically modifying and optimizing the structure of the substance, innovative drugs with better curative effect and fewer side effects may be developed. For example, after structural modification, it may improve the permeability of the drug to the blood-brain barrier, making it easier for the drug to reach the brain lesion area, thereby enhancing the therapeutic effect.
In the chemical industry, it plays a key role in the synthesis of polymer materials. It can be used as a functional monomer to participate in polymer polymerization reactions, giving the material unique properties. For example, it can be introduced into the synthesis process of polyester materials, which may improve the thermal stability and mechanical properties of the material. Due to the special groups it contains, it can form a strong interaction with the polyester molecular chain, enhancing the force between the molecular chains, thereby improving the overall performance of the material and meeting the high-performance requirements of materials in high-end fields such as aerospace and automotive manufacturing.
(3S-cis) -4-chlorobenzenesulfonic acid [5- (2,4-difluorophenyl) tetrahydro-5- (1H-1,2,4-triazole-1-ylmethyl) -3-furyl] methyl ester What are the precautions in the production process?
Preparation of (3S-cis) -4-hydroxyproline [5- (2,4-divinylphenyl) tetranitrogen-5- (1H-1,2,4-triazole-1-ylmethyl) - 3-imidazolyl] methyl ether has the following precautions in the production process:
First, the control of raw materials. It is necessary to ensure that (3S-cis) -4-hydroxyproline, 2,4-divinylphenyl related raw materials and 1,2,4-triazole-1-ylmethyl and other raw materials are of high quality and free of impurities. If there are impurities, or the reaction is skewed, the product is impure, such as impurities participating in the reaction, or by-products, disturbing the main reaction process, making it difficult to separate and purify the product.
Second, the consideration of reaction conditions. Temperature needs to be precisely controlled, and the reaction in different stages has different temperature effects. If the temperature is too high, it may cause overreaction, trigger side reactions, or even cause the decomposition of raw materials and products; if the temperature is too low, the reaction rate will be slow, time-consuming and lengthy, and the yield will decrease. The reaction time should also be strictly controlled. If the time is insufficient, the reaction will not be completed, and the amount of product will be small. If it takes too long, it may cause overreaction, which will damage the quality of the product.
Third, the consideration Choose the appropriate solvent to consider its effect on the solubility of the reactants and the reaction process. Good solvents can promote the contact of the reactants and facilitate the reaction; improper solvents, or resist the reaction. Choose the appropriate catalyst to increase the reaction rate and reduce the activation energy of the reaction. However, the amount of catalyst needs to be appropriate, too much or too little, both affect the reaction effect.
Fourth, the operation process is rigorous. The order of adding raw materials is particular, and the improper order or the reaction start is not good. Stirring should be uniform, so that the reactants are fully mixed and the reaction is uniform. The reaction equipment must be clean and free from the introduction of impurities. When separating and purifying the product, choose the appropriate method, such as recrystallization, column chromatography, etc., to achieve the purpose of high
What are the market prospects for (3S-cis) -4-chlorobenzenesulfonic acid [5- (2,4-difluorophenyl) tetrahydro-5- (1H-1,2,4-triazole-1-ylmethyl) -3-furyl] methyl ester?
(3S-cis) - 4 -hydroxyphenylacetic acid [5 - (2,4 -divinylphenyl) tetrazol - 5 - (1H - 1,2,4 -triazole - 1 -ylmethyl) - 3 -pyridyl] methyl ether What is the market prospect?
Guanfuji (3S-cis) -4-hydroxyphenylacetic acid [5- (2,4-divinylphenyl) tetrazol-5- (1H-1,2,4-triazole-1-ylmethyl) -3-pyridyl] methyl ether is a unique compound in the field of organic chemistry. Its structure is exquisite and composed of many parts.
In the field of medicine, its structure contains specific functional groups or has affinity for specific receptors, which in turn shows unique biological activities. For example, the hydroxyphenylacetic acid part of it may participate in the biochemical reactions of the human body and affect the enzymes or signaling pathways related to certain diseases. And structures such as triazolyl and pyridyl may also work synergistically to provide new opportunities for drug research and development. Today, the pharmaceutical industry has an increasing demand for new, efficient and low-toxicity drugs. If this compound can be further studied to confirm its pharmacological activity and safety, it will surely find a place in the pharmaceutical market, or become a key drug for the treatment of specific diseases, with promising prospects.
In the field of materials science, the unique structure of this compound may endow it with special physicochemical properties. For example, in photoelectric materials, its conjugate structure may affect the electron transport performance. If it is properly regulated, it may be applied to organic Light Emitting Diodes (OLEDs), solar cells and other fields. At present, materials science is constantly seeking new materials with excellent performance. If this compound can meet the relevant performance requirements, it will surely emerge in the material market and promote technological innovation in related fields.
However, its market prospects are not smooth sailing. On the one hand, the synthesis process of compounds may be complex, and cost control becomes the key. If efficient and low-cost synthesis cannot be achieved, large-scale production and marketing activities will be hindered. On the other hand, safety and environmental friendliness need to be strictly evaluated. In today's era of environmental protection and health, it is difficult to gain market recognition if it cannot meet relevant standards. But overall, with in-depth research and rational development, the market prospect of this compound is still promising.
What are the synthetic methods of (3S-cis) -4-chlorobenzenesulfonic acid [5- (2,4-difluorophenyl) tetrahydro-5- (1H-1,2,4-triazole-1-ylmethyl) -3-furyl] methyl ester?
To prepare (3S-cis) -4-bromobenzenesulfonic acid [5- (2,4-diethylphenyl) tetranitrogen-5- (1H-1,2,4-triazole-1-ylmethyl) -3-pyridyl] methyl sulfonamide, there are several methods. This synthesis method requires many steps and skills.
The choice of raw materials, 2,4-diethylbenzene, 1,2,4-triazole-1-ylmethyl related reagents, etc. are all important starting materials. At the beginning of the reaction, benzene compounds containing suitable substituents can be interacted with bromine reagents to introduce bromine atoms to obtain bromine-containing intermediates. This step requires controlling the reaction conditions, such as temperature, solvent, etc., so that bromine is substituted at the desired position to obtain an analogue of (3S-cis) -4-bromobenzene.
Then, react with a sulfonating reagent to obtain (3S-cis) -4-bromobenzene sulfonic acid. In this process, pay attention to the position and selectivity of the sulfonic acid group introduction, so that the sulfonic acid group is accurately connected to the target check point.
For the construction of the 5- (2,4-diethylphenyl) tetranitrogen moiety, the tetranitrogen structure can be introduced by a substrate containing diethylphenyl through a multi-step reaction. For example, by suitable nitrogen-containing reagents, under suitable conditions, the tetranitrogen ring system is gradually formed, and the 2,4-diethylphenyl group is properly connected to it.
And 5- (1H - 1,2,4 - triazole - 1 - ylmethyl) - 3 - pyridyl moiety, the compound containing the pyridyl group can be prepared first, and then the 1,2,4 - triazole - 1 - ylmethyl is introduced into the appropriate position of the pyridine ring. This step can be achieved by means of reactions such as nucleophilic substitution, pay attention to the reactivity and selectivity, and make the substituent access accurate check point.
Finally, the above parts are connected with appropriate reactions, such as condensation reactions, to form the target product (3S-cis) -4-bromobenzenesulfonic acid [5- (2,4-diethylphenyl) tetranitrogen-5- (1H-1,2,4-triazole-1-ylmethyl) -3-pyridyl] methylsulfonamide. Each step requires precise control of conditions, including temperature, pH, reaction time, etc., and proper separation and purification of intermediate products to ensure the purity and yield of the final product.