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What is the chemical structure of 2- [4- (1,3-benzodioxane-5-ylmethyl) piperazine-1-yl] pyrimidine methanesulfonate (1:1)
This is a difficult problem in organic chemistry. To solve the chemical structure of 2 - [4 - (1,3 - naphthaleno-dioxacyclopentene-5-ylmethyl) indole-1 - yl] propyl acrylate (1:1), it needs to be carefully analyzed.
First look at its main structure, "propyl acrylate", which is an ester structure containing double bonds. The acrylate part, containing a carbon-carbon double bond and an ester group, is the active check point of the polymerization reaction. The propyl group is the connecting group, which connects the main body with other complex structures.
Further exploration of the "2- [4- (1,3-naphthaleno-dioxane-5-ylmethyl) indole-1-yl]" part. The indole structure is a nitrogen-containing fused cyclic aromatic hydrocarbon with unique electron cloud distribution and chemical activity. 1-yl indicates that the substituent is attached to the indole position 1. 4- (1,3-naphthaleno-dioxane-5-ylmethyl), which is the substituent of the indole position 4. 1,3-Naphthaleno-dioxacyclopentene is a fused heterocyclic ring containing a naphthalene ring and a dioxacyclopentene structure. The 5-ylmethyl group is shown to be connected with a methyl group at the 5-position of the heterocyclic ring, and this methyl group is then connected to the indole 4-position.
In general, the chemical structure of 2 - [4 - (1,3-naphthaleno-dioxacyclopentene-5-ylmethyl) indole-1-yl] propyl acrylate (1:1) is based on propyl acrylate as the main body, and a complex substituent containing indole and naphthaleno-dioxacyclopentene is connected by propyl group. The various components interact with each other, endowing the compound with unique physical and chemical properties, which may have potential application value in fields such as organic synthesis and materials science.
What are the physical properties of 2- [4- (1,3-benzodioxane-5-ylmethyl) piperazine-1-yl] pyrimidine methanesulfonate (1:1)
2-%5B4-%281%2C3-%E8%8B%AF%E5%B9%B6%E4%BA%8C%E6%B0%A7%E6%9D%82%E7%8E%AF%E6%88%8A%E7%83%AF-5-%E5%9F%BA%E7%94%B2%E5%9F%BA%29%E5%93%8C%E5%97%AA-1-%E5%9F%BA%5D%E5%98%A7%E5%95%B6%E7%94%B2%E7%A3%BA%E9%85%B8%E7%9B%90%281%3A1%29 is a complex chemical substance expression. It involves 1,3-naphthalene and heterocyclopentenone dioxide, which are organic compounds with specific structures and properties.
The physical properties of this substance are related to key characteristics such as appearance, melting point, solubility, etc. Its appearance is often a specific color and shape, or crystalline, or powdery, which varies according to the preparation conditions and purity.
The melting boiling point is affected by factors such as intermolecular forces and hydrogen bonds. Strong intermolecular forces and hydrogen bonds often cause a high melting boiling point. For example, many compounds containing similar structures have high melting boiling points due to close intermolecular interactions.
Solubility is also an important physical property. In organic solvents, such as ethanol, ether, etc., it may have a certain solubility. Due to the principle of similar miscibility, the molecule of this substance is similar to the polar phase of the organic solvent molecule, so that the two can be mixed with each other. In water, its solubility may be poor, because its molecular polarity is quite different from that of water.
The existence of structures such as 5-methyl-1-yl also affects the overall physical properties. The introduction of methyl groups may change the polarity and spatial structure of molecules, which in turn affects the melting boiling point and solubility. For example, the increase of methyl groups may enhance the non-polarity of molecules and increase the solubility in non-polar solvents.
As for the 2-%5B4-%281%2C3-%E8%8B%AF%E5%B9%B6%E4%BA%8C%E6%B0%A7%E6%9D%82%E7%8E%AF%E6%88%8A%E7%83%AF-5-%E5%9F%BA%E7%94%B2%E5%9F%BA%29%E5%93%8C%E5%97%AA-1-%E5%9F%BA%5D%E5%98%A7%E5%95%B6%E7%94%B2%E7%A3%BA%E9%85%B8%E7%9B%90%281%3A1%29 whole, its physical properties are the comprehensive result of the interaction of each part structure, which is of great significance in chemical research and practical application.
What is the use of 2- [4- (1,3-benzodioxane-5-ylmethyl) piperazine-1-yl] pyrimidine methanesulfonate (1:1)?
2-%5B4-%281%2C3-%E8%8B%AF%E5%B9%B6%E4%BA%8C%E6%B0%A7%E6%9D%82%E7%8E%AF%E6%88%8A%E7%83%AF-5-%E5%9F%BA%E7%94%B2%E5%9F%BA%29%E5%93%8C%E5%97%AA-1-%E5%9F%BA%5D%E5%98%A7%E5%95%B6%E7%94%B2%E7%A3%BA%E9%85%B8%E7%9B%90%281%3A1%29 is a rather complex chemical substance expression. The use of this substance should be explored from its chemical composition and characteristics according to the concept of Tiangong Kaiji.
1,3-benzo-dicyclopentene-5-ylmethyl and other groups give this substance specific chemical activity and physical properties. The groups in this substance interact with each other, or make it have unique reactivity and stability.
In the chemical industry, such substances may be used as intermediates. Due to their complex structure and special groups, they can participate in many organic synthesis reactions and be converted into other more valuable compounds through specific chemical reaction pathways.
In the field of materials science, due to its special structure, it may be used to prepare materials with special properties. Its special groups may affect the electrical, optical or mechanical properties of materials, and then be used in electronic devices, optical materials and other fields.
Furthermore, its combination with acetic anhydride (1:1) may play a role in catalyzing or regulating the reaction process in some reactions. Special groups interact with acetic anhydride, or change the rate and selectivity of the reaction, which is of great significance in fine chemical synthesis.
In this way, such complex chemical substances may have a wide range of uses in many fields such as organic synthesis and material preparation. According to their structural characteristics, the reaction can be rationally designed to explore their potential application value.
What is the synthesis method of 2- [4- (1,3-benzodioxane-5-ylmethyl) piperazine-1-yl] pyrimidine methanesulfonate (1:1)
To prepare 2 - [4 - (1,3 - naphthaleno heterocyclopentene dioxide - 5 - methyl - 1 - yl) heptyl - 1 - yl] heptyl acrylate (1:1), the synthesis method is as follows:
First, the required raw materials need to be prepared, including naphthalene and heterocyclopentene dioxide derivatives with specific structures, reactants with heptyl structures and acrylate related reagents.
In the reactor, a suitable organic solvent is used as the medium, such as toluene, dichloromethane, etc., to create a suitable reaction environment. Add an appropriate amount of catalyst, such as p-toluenesulfonic acid, to promote the reaction.
Mix the raw material containing naphthalene and heterocyclopentene dioxide with the reactant containing heptyl group in an appropriate ratio, and stir the reaction at a certain temperature. Temperature control is critical, or it needs to be maintained between 50 and 80 degrees Celsius, and the reaction time is about several hours, so that the two can fully react to form an intermediate product.
Subsequently, this intermediate product is mixed with an acrylate reagent, and can be reacted at a suitable temperature (or 40-60 degrees Celsius) under the action of an alkaline catalyst, such as potassium carbonate, etc. The purpose of this step is to esterify the intermediate product with the acrylate to form the target product 2 - [4 - (1,3 - naphthalene heterocyclopentene dioxide - 5 - methyl - 1 - yl) heptyl - 1 - yl] heptyl acrylate (1:1).
After the reaction is completed, the product is separated and purified by conventional separation methods, such as extraction, column chromatography, etc., and impurities are removed to obtain a high-purity target product. In this way, the synthesis of this compound is completed.
What are the applications of 2- [4- (1,3-benzodioxane-5-ylmethyl) piperazine-1-yl] pyrimidine methanesulfonate (1:1) in the field of medicine?
2-%5B4-%281%2C3-%E8%8B%AF%E5%B9%B6%E4%BA%8C%E6%B0%A7%E6%9D%82%E7%8E%AF%E6%88%8A%E7%83%AF-5-%E5%9F%BA%E7%94%B2%E5%9F%BA%29%E5%93%8C%E5%97%AA-1-%E5%9F%BA%5D%E5%98%A7%E5%95%B6%E7%94%B2%E7%A3%BA%E9%85%B8%E7%9B%90%281%3A1%29 is a rather complex chemical substance expression. This compound has many applications in the field of medicine.
It is often used as a key intermediate in the field of drug synthesis. Due to its unique chemical structure, compounds with diverse biological activities can be constructed through specific chemical reactions. Taking the development of anti-cancer drugs as an example, scientists synthesized a series of derivatives by modifying and modifying the structure of the substance, and experimentally screened out new anti-cancer drugs that have significant inhibitory effects on the proliferation of cancer cells.
In anti-infective drugs, 2-%5B4-%281%2C3-%E8%8B%AF%E5%B9%B6%E4%BA%8C%E6%B0%A7%E6%9D%82%E7%8E%AF%E6%88%8A%E7%83%AF-5-%E5%9F%BA%E7%94%B2%E5%9F%BA%29%E5%93%8C%E5%97%AA-1-%E5%9F%BA%5D%E5%98%A7%E5%95%B6%E7%94%B2%E7%A3%BA%E9%85%B8%E7%9B%90%281%3A1%29 also has applications. It can be used as a starting material to prepare drugs that inhibit or kill pathogens such as bacteria and viruses through multi-step reactions. For example, in the synthesis of some new antibiotics, the substance participates in the reaction, providing a key structural unit for the construction of antibiotic molecules with unique antibacterial mechanisms, enhancing the antibacterial activity and specificity of the drug, and reducing the generation of drug resistance.
This compound also plays an important role in the development of drugs for the treatment of nervous system diseases. By adjusting its chemical structure, substances with specific affinity for neurotransmitter receptors can be obtained for the treatment of neurodegenerative diseases such as Parkinson's disease and Alzheimer's disease. Scientists use its structural properties to design and synthesize drugs that can modulate neurotransmitter transmission and improve nerve cell function, providing new strategies and drug options for the treatment of nervous system diseases.