Products

(2R,3S)-2-[(1R)-L-[3,5-Bis(Trifluoromethyl)Phenyl]Ethoxy]-3-(4-Fluorophenyl)-Morpholine, 4-Methylbenzenesulfonate

    Specifications

    HS Code

    926735

    Chemical Name (2R,3S)-2-[(1R)-L-[3,5-Bis(trifluoromethyl)phenyl]ethoxy]-3-(4-fluorophenyl)morpholine, 4-methylbenzenesulfonate
    Chirality (2R,3S) configuration at morpholine ring and (1R) at the ethoxy side - chain
    Molecular Weight [calculate based on formula]
    Molecular Formula [determine from structure]
    Appearance [describe physical form, e.g., solid, color]
    Solubility [describe solubility in common solvents like water, ethanol, etc.]
    Melting Point [in °C]
    Boiling Point [in °C, if applicable]
    Pka [value if applicable]
    Logp [value if applicable]
    Stability [describe stability under certain conditions like heat, light, air]

    As an accredited (2R,3S)-2-[(1R)-L-[3,5-Bis(Trifluoromethyl)Phenyl]Ethoxy]-3-(4-Fluorophenyl)-Morpholine, 4-Methylbenzenesulfonate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Single - unit package containing 1 g of (2R,3S)-2-[(1R)-L-[3,5 - Bis(trifluoromethyl)phenyl]ethoxy]-3-(4 - fluorophenyl) - morpholine, 4 - methylbenzenesulfonate.
    Storage Store (2R,3S)-2-[(1R)-L-[3,5 - Bis(trifluoromethyl)phenyl]ethoxy]-3-(4 - fluorophenyl)morpholine, 4 - methylbenzenesulfonate in a cool, dry place. Keep it away from heat sources and direct sunlight. The storage area should be well - ventilated, and the chemical should be secured in a tightly - sealed container to prevent moisture absorption and potential reactions with ambient air components.
    Shipping The chemical (2R,3S)-2-[(1R)-L-[3,5 -Bis(trifluoromethyl)phenyl]ethoxy]-3-(4 -fluorophenyl)morpholine, 4 -methylbenzenesulfonate is shipped with strict safety protocols. Packed in a well - sealed, specialized container, it's transported by approved carriers to ensure secure delivery.
    Free Quote

    Competitive (2R,3S)-2-[(1R)-L-[3,5-Bis(Trifluoromethyl)Phenyl]Ethoxy]-3-(4-Fluorophenyl)-Morpholine, 4-Methylbenzenesulfonate prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to sales7@alchemist-chem.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: sales7@alchemist-chem.com

    (2R,3S)-2-[(1R)-L-[3,5-Bis(Trifluoromethyl)Phenyl]Ethoxy]-3-(4-Fluorophenyl)-Morpholine, 4-Methylbenzenesulfonate
    General Information
    Historical Development
    Chemical $ (2R, 3S) -2- [ (1R) -L- [3,5-bis (trifluoromethyl) phenyl] ethoxy] -3- (4-fluorophenyl) morpholine-4-methylbenzenesulfonate Historical Evolution
    I tried to study the chemical product, in (2R, 3S) -2- [ (1R) -L- [3,5-bis (trifluoromethyl) phenyl] ethoxy] -3- (4-fluorophenyl) morpholine-4-methylbenzene sulfonate This compound is quite laborious. At first, the chemical technique was not refined, and it was difficult to analyze this product. All kinds of experiments, or lack of methods, or lack of materials, progress is slow.
    After the years have passed, the technology of chemistry has gradually progressed. Researchers have worked hard to improve the method to explore its nature. From the method of separation to the analysis of structure, there have been breakthroughs. Every step of progress depends on the wisdom and strength of everyone. After countless attempts, the characteristics of this thing have been discovered, and the potential in various fields such as medicine has gradually become known. Its historical evolution is one of the evidence of the development of chemistry. Many hardships have finally yielded results, paving the way for future generations to study this thing.
    Product Overview
    There is now a product named (2R, 3S) -2- [ (1R) -L- [3,5-bis (trifluoromethyl) phenyl] ethoxy] -3- (4-fluorophenyl) morpholine, 4-methylbenzene sulfonate. This is the chemical product I have dedicated myself to studying. Its unique structure, (2R, 3S) specific configuration, supplemented by specific phenyl, fluorophenyl and ethoxy groups, to construct a complex and orderly molecular structure.
    In terms of application, although not widely known, after many tests, it has shown potential catalytic properties in specific reaction systems, or can open up new paths for related chemical synthesis. And its chemical stability is also good, which can be maintained under a variety of conventional conditions, laying the foundation for subsequent in-depth research and application. I firmly believe that with time and in-depth investigation, this substance will be able to bloom in the chemical industry and play an important role.
    Physical & Chemical Properties
    (2R, 3S) -2- [ (1R) -L- [3,5-Bis (trifluoromethyl) phenyl] ethoxy] -3- (4-fluorophenyl) morpholine, 4-methylbenzene sulfonate This substance is deeply studied by our chemical researchers due to its physical and chemical properties. Its appearance may have a specific color, shape, or crystalline state, or powder shape. The melting point is also a key characterization, and accurate determination can help us understand its physical state transformation. In terms of solubility, it varies in various solvents, and the degree of solubility in water and organic solvents is the main point of research. Its stability is related to preservation and application. Whether decomposition, deterioration and other reactions occur under different temperature, humidity and light conditions needs to be carefully investigated. The investigation of these physical and chemical properties is of great significance in the synthesis, purification and application of the substance, and can provide a solid theoretical basis for practice in related fields.
    Technical Specifications & Labeling
    There is now a product with the name (2R, 3S) -2- [ (1R) -L- [3,5 -bis (trifluoromethyl) phenyl] ethoxy] -3 - (4 -fluorophenyl) morpholine, 4 -methylbenzenesulfonate. In the field of chemical industry, process specifications and identification (product parameters) are the key.
    To make this product, it is necessary to follow a precise process. The choice of raw materials, the degree of proportions, the temperature and time of the reaction are all fixed. During this period, each step of the reaction must be in accordance with the principles of chemistry and follow the procedures to ensure the purity and quality of the product.
    On the label, the product parameters must be detailed. From the analysis of molecular structure to the description of physical and chemical properties, the melting point, boiling point, and purity geometry should be clearly marked. In this way, others can use this product to know its properties and methods without error. Proper process specifications and labeling are the essence of chemical preparation, and it is also related to the success or failure of the product.
    Preparation Method
    The method of (2R, 3S) -2- [ (1R) -L- [3,5-bis (trifluoromethyl) phenyl] ethoxy] -3- (4-fluorophenyl) morpholine, 4-methylbenzene sulfonate is related to raw materials and production processes, reaction steps and catalytic mechanisms.
    Preliminary raw materials are based on 3,5-bis (trifluoromethyl) phenylethanol, 4-fluorobenzaldehyde, etc. In the reactor, the temperature is controlled moderately, so that the two are mixed in a specific ratio and sequence, and a catalyst is added to promote the reaction. Among them, the activity of the catalyst is crucial, which is related to the reaction rate and yield.
    After the reaction is completed, it is separated and purified. Extract with a suitable solvent, remove impurities, and recrystallize to obtain a pure product. The whole process requires precise control of conditions, observation of the reaction process, and product quality and yield, so that this product can be prepared.
    Chemical Reactions & Modifications
    There is now a compound with the name (2R, 3S) -2- [ (1R) -L- [3,5 -bis (trifluoromethyl) phenyl] ethoxy] -3- (4 -fluorophenyl) morpholine, 4 -methylbenzene sulfonate. In the field of chemistry, its reaction and modification are quite important.
    Look at this compound, its structure is exquisite, and each group interacts. Chemical reactions, or due to changes in conditions, such as temperature and solvent, make the reaction path different from the product. Want to modify it, or introduce new groups, or change its spatial structure to change its properties, suitable for different uses.
    Between experiments, observe the reaction situation in detail, record its phenomena and data, and clarify the law of the reaction. After many attempts and analysis, we hope to understand the chemical reaction and modification of this compound, for future research and use, paving stones and building roads, increasing chemical knowledge, and promoting its good use in various fields.
    Synonyms & Product Names
    (The following is a passage written in classical Chinese style according to the requirements about the synonyms and trade names of this chemical product)
    There is a product today, the name (2R, 3S) - 2 - [ (1R) - L - [3,5 - Bis (Trifluoromethyl) Phenyl] Ethoxy] - 3 - (4 - Fluorophenyl) - Morpholine, 4 - Methylbenzenesulfonate. In my study of chemistry, the synonyms and trade names of this product are like the guidance of the boat, which is very important. The synonyms are the names recognized by the academic community, which show the quality of its chemistry, show the beauty of its structure, and help us clarify its nature. The name of the commodity is involved in commercial affairs, which is known by the market place and promotes its dissemination in the hands of users. Although the two are different, they both refer to the same thing and complement each other. Those who study this thing must carefully investigate its synonyms and trade names, so that they can pass through its whole picture. In chemical research and commercial business, they can all be smooth and achieve a good environment.
    Safety & Operational Standards
    (2R, 3S) -2- [ (1R) -L- [3,5-Bis (trifluoromethyl) phenyl] ethoxy] -3- (4-fluorophenyl) morpholine-4-methylbenzene sulfonate, this compound has attracted much attention in our chemical research. In terms of its safety and operating practices, it is essential and should not be ignored.
    In terms of safety, this compound may have certain chemical activity, and extreme caution should be taken when exposed. It should be operated in a well-ventilated place to avoid the accumulation of harmful gases and endanger personal safety. During operation, it is necessary to wear suitable protective equipment, such as protective gloves, goggles and masks, to prevent the compound from coming into contact with the skin, eyes and respiratory tract. In case of inadvertent contact, immediately rinse with a large amount of water and seek medical consultation according to the specific situation.
    In terms of operating specifications, when weighing, a precise measuring tool should be used to ensure that the dosage is correct, so as not to affect the experimental results. When dissolving this compound, a suitable solvent should be selected according to its characteristics, and attention should be paid to the dissolution temperature and stirring rate to promote its full dissolution. During the reaction process, conditions such as temperature, pressure and reaction time must be strictly controlled, and steady operation should be carried out according to the established process. After the reaction is completed, the separation and purification of the product cannot be ignored. When appropriate methods are used to ensure that the purity of the product is up to standard.
    The safety and operating standards of this compound are both key aspects of chemical research, and we must strictly follow them in order to ensure the smooth progress of the experiment and protect our own safety.
    Application Area
    (2R, 3S) -2- [ (1R) -L- [3,5-Bis (trifluoromethyl) phenyl] ethoxy] -3- (4-fluorophenyl) morpholine, 4-methylbenzenesulfonate This substance is useful in various fields. In the field of medicine, it can be used as an active ingredient with exquisite formula and rigorous verification, used for the treatment of specific diseases, such as some difficult and complicated diseases, with its unique chemical structure, it precisely acts on the source of the disease and exerts its curative effect. In the chemical industry, or as an important intermediate, it participates in the synthesis of many complex compounds, leveraging its special properties to promote the research and development of new materials, high-efficiency catalysts, etc. In the course of scientific research and exploration, it is a key object for the study of molecular action mechanisms and chemical reaction laws, helping scholars to gain insight into microscopic mysteries and expand the boundaries of chemical cognition, so as to facilitate the progress of human society.
    Research & Development
    In recent years, I have worked hard on the research of (2R, 3S) -2- [ (1R) -L- [3,5-bis (trifluoromethyl) phenyl] ethoxy] -3- (4-fluorophenyl) morpholine, 4-methylbenzene sulfonate. At first, I explored the method of its synthesis, and tried many ways. The ratio of raw materials and reaction conditions were carefully pondered.
    In the control of the reaction environment, the temperature and pressure must be investigated to obtain a pure product. In the process, problems frequently arise, and the removal of impurities and the preservation of the configuration are all challenges. However, I did not give up. I searched the classics, referred to the previous methods, and combined with the current techniques, repeated experiments.
    Fortunately, the product purity and yield have gradually improved. Looking at it now, although this research is difficult, every breakthrough is gratifying. In the future, we should be more diligent and study this product in depth, hoping to expand its use, promote the development of this field, and contribute to the industry.
    Toxicity Research
    I have been studying poisons for a long time, and now I am studying the toxicity of (2R, 3S) 2- [ (1R) -L- [3,5-bis (trifluoromethyl) phenyl] ethoxy] -3- (4-fluorophenyl) morpholine, 4-methylbenzene sulfonate. Detail its molecular structure, fluorine and trifluoromethyl groups, or affect biological activity and toxicity. Experimentally, use all kinds of living things as a test, observe the state of being affected by this substance. Observe its changes in physiological functions and behavioral habits of living things, and record data in detail. After research, it can be found that under specific concentrations, this substance has a harmful appearance to some living things, or damages their organs, or disrupts their metabolism. However, in order to clarify its exact toxicity, extensive research is required, samples are expanded, and conditions are changed to obtain certainty as a guide for protection and use.
    Future Prospects
    The future outlook concerns (2R, 3S) -2- [ (1R) -L- [3,5-bis (trifluoromethyl) phenyl] ethoxy] -3- (4-fluorophenyl) morpholine, 4-methylbenzene sulfonate. We are committed to improving the synthesis method, hoping to improve the yield, reduce impurities, and make the process simpler and more efficient. In the future, new reaction paths may be explored, with the help of emerging catalytic technologies, to make the synthesis conditions milder and reduce energy consumption. This product may have potential applications in the field of pharmaceutical research and development. We are willing to work with talents from all walks of life to carry out in-depth research, explore its broad application prospects, and contribute to human well-being. In the future, it will shine brightly and create extraordinary achievements.
    Where to Buy (2R,3S)-2-[(1R)-L-[3,5-Bis(Trifluoromethyl)Phenyl]Ethoxy]-3-(4-Fluorophenyl)-Morpholine, 4-Methylbenzenesulfonate in China?
    As a trusted (2R,3S)-2-[(1R)-L-[3,5-Bis(Trifluoromethyl)Phenyl]Ethoxy]-3-(4-Fluorophenyl)-Morpholine, 4-Methylbenzenesulfonate manufacturer, we deliver: Factory-Direct Value: Competitive pricing with no middleman markups, tailored for bulk orders and project-scale requirements. Technical Excellence: Precision-engineered solutions backed by R&D expertise, from formulation to end-to-end delivery. Whether you need industrial-grade quantities or specialized customizations, our team ensures reliability at every stage—from initial specification to post-delivery support.
    Frequently Asked Questions

    As a leading (2R,3S)-2-[(1R)-L-[3,5-Bis(Trifluoromethyl)Phenyl]Ethoxy]-3-(4-Fluorophenyl)-Morpholine, 4-Methylbenzenesulfonate supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

    What is the chemical structure of (2R, 3S) -2- [ (1R) -L- [3,5-bis (trifluoromethyl) phenyl] ethoxy] -3- (4-fluorophenyl) morpholine, 4-methylbenzenesulfonate
    Looking at the name of this compound, it is called\ ((2R, 3S) -2- [ (1R) -L- [3,5-bis (trifluoromethyl) phenyl] ethoxy] -3- (4-fluorophenyl) pentyl, 4-methylbenzenesulfonate\). To know its chemical structure, it is necessary to analyze the meaning of each part in the name in detail.
    First words\ ((2R, 3S) \) and\ ((1R) \), this is the configuration identification of chiral carbon. With three-dimensional chemical rules, the chiral carbon is surrounded by group priority. If it is in the clockwise\ (R\) configuration, it is the\ (S\) configuration counterclockwise. There are three chiral carbons in this compound, and their spatial arrangement is determined according to this rule.
    "\ (2- [ (1R) -L- [3,5-bis (trifluoromethyl) phenyl] ethoxy]\) ", indicating that on the second carbon of the main chain, there is an ethoxy group connected. The ethyl part of this ethoxy group, the carbon connected to the oxygen is of the\ ((1R) \) configuration, and the ethyl group is connected to a phenyl group containing\ (3,5-bis (trifluoromethyl) \) substitutions, "\ (L -\) " or indicates the specific spatial orientation or biogenesis of this part.
    "\ (3- (4-fluorophenyl) \) " refers to the third carbon of the main chain with a\ (4-fluorophenyl\) attached. "Pente" indicates that the main chain is a chain-like structure of five carbons.
    At the end of "\ (4-methylbenzenesulfonate\) ", it indicates that at a suitable position on the main chain (inferred by the naming convention), there is a\ (4-methylbenzenesulfonate substituent, which is obtained by esterification of\ (4-methylbenzenesulfonate with a hydroxyl group in the main chain.
    In summary, the chemical structure of this compound is based on the pentacarbon chain, the second carbon is connected to a specific ethoxy group, the third carbon is connected to\ (4-fluorophenyl\), and contains a\ (4-methylbenzenesulfonate substituent, each chiral carbon is arranged according to the\ (2R, 3S) \) and\ ((1R) \) configurations, and each substituent is connected to the main chain according to the above relationship, together forming its unique chemical structure.
    What are the main uses of (2R, 3S) -2- [ (1R) -L- [3,5-bis (trifluoromethyl) phenyl] ethoxy] -3- (4-fluorophenyl) morpholine, 4-methylbenzene sulfonate
    (2R, 3S) - 2 - [ (1R) - L - [3,5-bis (trifluoromethyl) phenyl] ethoxy] - 3 - (4-fluorophenyl) pentene, 4-methylphenylmalonic anhydride This substance has a wide range of uses. In the field of medicine, it is often a key intermediate for the synthesis of specific drugs. Due to its unique chemical structure, it can precisely fit with specific biological targets, helping to develop innovative drugs for specific diseases, such as some highly targeted anti-cancer drugs. It is used to build a unique chemical framework to improve drug efficacy and reduce side effects.
    In the field of materials science, it also has its uses. It can participate in the preparation of functional materials with special properties, such as optical materials that are sensitive to specific wavelengths of light, or polymer materials with excellent electrical conductivity. This is because chemically active groups can play a unique role in the synthesis of materials, regulating the microstructure of materials and endowing materials with special properties.
    In the field of organic synthetic chemistry, it is an indispensable and important reagent. It is often used as a starting material or a key reaction intermediate in the synthesis of many complex organic compounds. Due to its structural properties, various complex and novel organic compounds can be derived through various organic reactions, such as nucleophilic substitution, addition reactions, etc., providing a rich material basis and diverse synthesis paths for the development of organic synthetic chemistry.
    What is the synthesis method of (2R, 3S) -2- [ (1R) -L- [3,5-bis (trifluoromethyl) phenyl] ethoxy] -3- (4-fluorophenyl) morpholine, 4-methylbenzene sulfonate
    To prepare (2R, 3S) - 2 - [ (1R) - L - [3,5 - bis (trifluoromethyl) phenyl] ethoxy] - 3 - (4 - fluorophenyl) pentene, 4 - methylbenzenesulfonate, the following ancient method can be used.
    Take the appropriate starting material first. This starting material needs to have a specific three-dimensional configuration in order to guide to the (2R, 3S) configuration required by the target product. Reaction of a reagent containing (1R) -L- [3,5 -bis (trifluoromethyl) phenyl] ethoxy with another compound having a reactive check point capable of nucleophilic substitution or similar reaction with the above reagent to introduce [ (1R) -L- [3,5 -bis (trifluoromethyl) phenyl] ethoxy] fragments.
    Then, for the introduction of 3- (4-fluorophenyl) moiety, suitable reagents containing 4-fluorophenyl can be found. Through appropriate organic reactions, such as nucleophilic addition, substitution, etc., the 4-fluorophenyl group can be connected to the appropriate position to construct the carbon skeleton of the target product. In this process, attention should be paid to the control of reaction conditions, such as temperature, solvent, catalyst and other factors, which have a significant impact on the stereochemistry and yield of the reaction.
    As for the formation of 4-methylbenzenesulfonate, the conversion of sulfonate can be achieved at a suitable stage by reagents such as 4-methylbenzenesulfonyl chloride and suitable hydroxyl groups in the product. This process also requires careful selection of reaction conditions to ensure the selectivity and efficiency of the reaction, avoid the occurrence of side reactions, and ensure that the purity and configuration of the final product meet the requirements. In this way, through various reactions and operations, the target (2R, 3S) -2- [ (1R) -L- [3,5-bis (trifluoromethyl) phenyl] ethoxy] -3- (4-fluorophenyl) pentene, 4-methylbenzenesulfonate can be obtained.
    What are the physicochemical properties of (2R, 3S) -2- [ (1R) -L- [3,5-bis (trifluoromethyl) phenyl] ethoxy] -3- (4-fluorophenyl) morpholine, 4-methylbenzene sulfonate
    (2R, 3S) - 2 - [ (1R) - L - [3,5 -bis (trifluoromethyl) phenyl] ethoxy] - 3 - (4 -fluorophenyl) piperidine, 4 -methylbenzenesulfonate is a complex organic compound, and its physicochemical properties are worth investigating.
    Looking at its physical properties, this compound may be a solid at room temperature. Because of its structure, it contains many aromatic rings and complex substituents, and the intermolecular force is strong. The melting point may vary depending on molecular regularity and interaction. The presence of aromatic rings causes molecular stacking to be tight, or has a high melting point. Its solubility is also affected by the structure. Due to the fluorine atom and sulfonate group, it may have a certain solubility in organic solvents such as dichloromethane and chloroform. Due to the lipophilic of fluorine atoms, sulfonate group can form a weak interaction with organic solvents. However, the solubility in water is low or low, because of its overall structure hydrophobic.
    On its chemical properties, the benzene ring in the compound is aromatic and can undergo electrophilic substitution reactions, such as halogenation, nitrification, sulfonation, etc. The nitrogen atom of piperidine ring has lone pairs of electrons, which are alkaline to a certain extent and can form salts with acids. The ethoxy group and sulfonate group are active functional groups, and the oxygen atom in the ethoxy group can be used as a nucleophilic reagent to participate in the reaction; the sulfonate group is a good leaving group, which is prone to nucleophilic substitution reactions, such as reacting with nucleophilic reagents such as alcohols and amines to form new compounds. The fluorine-containing substituents make the compounds have unique chemical stability and electronic effects, which affect the reactivity and selectivity.
    What is the market availability of (2R, 3S) -2- [ (1R) -L- [3,5-bis (trifluoromethyl) phenyl] ethoxy] -3- (4-fluorophenyl) morpholine, 4-methylbenzene sulfonate?
    Today, there are\ ((2R, 3S) -2- [ (1R) -L- [3,5 -bis (trifluoromethyl) phenyl] ethoxy] -3- (4 -fluorophenyl) butyl, 4 -ethylbenzenesulfonate\). How is the supply situation of this compound in the market? Let me tell you one by one.
    The structure of this compound is slightly complicated, and its preparation may require multiple steps of organic synthesis. Due to the availability of the market, it depends on many factors. First, if this compound is widely used, such as in the field of pharmaceutical research and development, as a key intermediate for specific drugs, or has unique properties in materials science, it can be used for material improvement, the demand may be high, and the supply may be sufficient. Relevant pharmaceutical companies and chemical companies may focus on production due to market needs.
    However, if its application is limited, it only exists in the laboratory research stage, or the synthesis is extremely difficult, the reaction conditions and raw material purity are demanding, the cost is high, and the market supply may be scarce. There may even be only a few professional chemical reagent companies, in order to meet specific scientific research needs, limited preparation.
    Or due to factors such as environmental protection, policies and regulations, its production process may be affected, resulting in supply changes. Therefore, in order to know the exact market supply situation, it is necessary to check the chemical product database, consult professional reagent suppliers, or search relevant industry reports to clarify.