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What is the chemical structure of 2 (S) - [4- (3-fluorobenzyloxy) benzylamino] propionamide methanesulfonate
My question is about the chemical structure of (2S) - [4- (3-hydroxyethyl) piperazinyl] ethyl butyrate hydrochloride. The structure of this compound depends on the principles of organic chemistry.
(2S) - [4- (3-hydroxyethyl) piperazinyl] ethyl butyrate hydrochloride, the structural core of which is a piperazine ring. The piperazine ring has the shape of a six-membered nitrogen-containing heterocycle, in which two nitrogen atoms are distributed opposite to each other. In the fourth position of this ring, there are 3-hydroxyethyl groups connected. This 3-hydroxyethyl group is an ethyl-terminated hydroxyl group, and the hydroxyl group has active chemistry and can be involved in many reactions.
The other nitrogen atom of the piperazine ring is connected to the structure of ethyl butyrate. Ethyl butyrate is obtained by esterification of butyric acid and ethanol. Butyric acid contains a straight-chain carboxylic acid containing four carbons, and its carboxyl group is esterified with the hydroxyl group of ethanol to form an ester group. The existence of this ester group gives the molecule specific physical and chemical properties.
As for (2S), it means that the compound has chirality and the configuration is S-type. Chirality is very important in organic chemistry, and things of different configurations may have different biological activities.
The state of hydrochloride is due to the lone pair of electrons in the nitrogen atom in the compound, which can combine with the hydrogen ion of hydrochloric acid to form a salt. This salt state can increase the solubility and other properties of the compound.
In short, the structure of (2S) - [4- (3-hydroxyethyl) piperazinyl] ethyl butyrate hydrochloride is composed of piperazine ring, 3-hydroxyethyl, ethyl butyrate and hydrochloride. The parts interact with each other, giving this compound its unique chemistry and potential applications.
What are the main uses of 2 (S) - [4- (3-fluorobenzyloxy) benzylamino] propionamide methanesulfonate
2% 28S% 29- [4- (3-hydroxyamino) ureylureyl] succinic anhydride, the main uses of this compound are as follows:
First, in the field of pharmaceutical research and development, its structural properties make it have the potential to participate in the design and synthesis of drug molecules. It may serve as a key intermediate, and through specific chemical reactions, complex molecular structures with specific pharmacological activities can be constructed. For example, for some disease targets, through chemical modification and modification, it is expected to develop new therapeutic drugs, which will play an important role in the development of anti-cancer, anti-infection and many other diseases.
Second, in the field of materials science, this compound can participate in the synthesis of polymer materials as a functional monomer. With its special functional groups, it can endow materials with unique properties, such as improving the hydrophilicity and biocompatibility of materials. For example, in biomedical materials, its good biocompatibility allows materials to better interact with biological tissues and reduce immune responses, which is then widely used in the preparation of wound dressings, tissue engineering scaffolds and other materials.
Third, in organic synthetic chemistry, it is an important type of synthetic building block. With its multi-functional group characteristics, it can participate in a variety of organic reactions, such as condensation reactions, addition reactions, etc., thus providing an effective way to synthesize complex and diverse organic compounds. Organic chemists can build organic molecules with different spatial structures and functional group distributions based on this compound, expanding the variety and properties of organic compounds.
Fourth, in the field of agricultural chemistry, it may be used to develop new pesticides or plant growth regulators. With the adjustment and optimization of its structure, pesticide products that have high-efficiency control of crop diseases and pests, are environmentally friendly and have low toxicity to non-target organisms; or plant growth regulators that can regulate plant growth and development, improve crop yield and quality.
What is the preparation method of 2 (S) - [4- (3-fluorobenzyloxy) benzylamino] propionamide methanesulfonate
To prepare 2% (S) - [4 - (3 - hydroxyethoxy) benzyloxy] butenolactone, the details are as follows.
First take an appropriate amount of starting material, which should have the basic structure related to the target product. In a clean reactor, dissolve it with a suitable organic solvent. The selected solvent must have good solubility to the reaction raw materials and intermediates, and do not side-react with the reactants.
Then, add a specific catalyst to it. This catalyst is the key to the reaction, which can effectively promote the reaction and reduce the activation energy required for the reaction. The amount of catalyst needs to be precisely controlled. Too much or too little will affect the rate and yield of the reaction.
During the reaction process, the temperature and time of the reaction need to be strictly controlled. If the temperature is too low, the reaction rate will be delayed or the reaction will be incomplete; if the temperature is too high, it may cause side reactions and reduce the purity of the product. Therefore, maintain a suitable temperature range, depending on the process and characteristics of the reaction, or under mild heating conditions, or at room temperature. Time cannot be ignored. It is necessary to closely observe the degree of the reaction and stop the reaction in time to obtain the ideal product.
After the reaction is completed, the reaction mixture will be treated. Separation and purification methods such as extraction, filtration, distillation, etc. can be used to remove unreacted raw materials, catalysts and by-products to obtain a pure target product of 2% (S) - [4- (3-hydroxyethoxy) benzyloxy] butenolactone. The whole process requires strict operation by the experimenter and follow the experimental specifications and procedures to successfully prepare.
What are the physical properties of 2 (S) - [4- (3-fluorobenzyloxy) benzylamino] propionamide methanesulfonate
"The physical properties of 2- [4- (3-hydroxyethylamino) ethylamino] ethyl-1-naphthalenesulfonic acid are light-colored and nearly transparent, mostly in powder or crystalline state, easily soluble in water, and also has a certain solubility in organic solvents. Its melting point is relatively clear, which can be used as evidence for identification. This substance has good stability, and it is not easy to decompose under normal conditions. However, in the case of strong acids, strong alkalis, or in the environment of high temperature and strong oxidation, the structure may be damaged, and the properties will be changed accordingly. And it has good surface activity and is useful in many fields, which is also its remarkable physical properties."
What are the precautions for the use of 2 (S) - [4- (3-fluorobenzoxy) benzylamino] propionamide methanesulfonate
2%28S%29-%5B4-%283-%E6%B0%9F%E8%8B%84%E6%B0%A7%E5%9F%BA%29%E8%8B%84%E5%9F%BA%E6%B0%A8%E5%9F%BA%5D%E4%B8%99%E9%85%B0%E8%83%BA%E7%94%B2%E7%A3%BA%E9%85%B8%E7%9B%90, this chemical substance should pay attention to the following points in use:
First, it is related to its toxicity. This substance may be toxic to a certain extent, and comprehensive protective measures must be taken when using it. Such as wearing professional protective clothing, protective gloves, wearing a gas mask, etc., to prevent the human body from coming into contact with it or inhaling its volatile gas, so as to avoid damage to the body, especially to the respiratory tract, skin and eyes, etc., more careful protection is required.
Second, about storage conditions. It should be stored in a cool, dry and well-ventilated place, away from fire and heat sources. Because of its chemical properties or cause it to be unstable in high temperature environments, and even cause dangerous reactions. At the same time, it should be stored separately from oxidizing agents, acids, alkalis and other substances to avoid adverse reactions caused by mixing with each other and endanger safety.
Third, the operation specifications during use. The operation should be strictly in accordance with the established procedures, and the action should be accurate and steady to avoid spilling, leakage and other conditions. If a leak unfortunately occurs, an emergency response plan should be initiated immediately, and irrelevant personnel should be quickly evacuated to a safe area, and the leakage area should be strictly isolated. According to the amount of leakage, choose an appropriate way to clean up, such as the use of inert materials for adsorption, and then properly collect and treat it harmlessly.
Fourth, for its transportation. During transportation, be sure to ensure that the packaging is complete and well sealed to prevent leakage during bumps and vibrations. Transportation vehicles need to be equipped with corresponding emergency treatment equipment and protective equipment, and transportation personnel should be familiar with the dangerous characteristics and emergency treatment methods of this substance to ensure safety during transportation.