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Deschloro-N-ethyl-Ketamine (hydrochloride), molecular formula C14H20ClNO, CAS 4551-92-2, relative molecular weight 274.2 g/mol. In solid state, it usually appears as a white to slightly yellow crystalline powder. This powder has fine particles, uniform texture, and no obvious impurities or color spots. Under illumination, its color may change slightly, but usually remains stable. At room temperature, it has low volatility and is not easy to evaporate into the air. However, under high temperature or vacuum conditions, its volatility may increase. Easy to dissolve in water, 1 gram can dissolve in 2 milliliters of water, and when dissolved in water, it can ionize chloride ions and corresponding cations, thus having a certain conductivity. Easily soluble in small amounts of methanol, chloroform, and acetone, insoluble in ethanol and ether. Stable and not easily decomposed or degraded when stored at room temperature. In research in fields such as neuroscience, pharmacology, and toxicology, this compound may be used as a tool compound. By observing and analyzing the impact of this compound on biological or cellular models, scientists can better understand the mechanisms of specific biological processes or diseases.
|
Chemical Formula |
C14H20ClNO |
|
Exact Mass |
253 |
|
Molecular Weight |
254 |
|
m/z |
253 (100.0%), 254 (15.1%), 255 (32.0%), 256 |
|
Elemental Analysis |
C, 66.26; H, 7.94; N, 5.52; O, 6.03; Cl, 1.97 |
There are several ways to synthesize deschloro-N-ethyl-Ketamine (hydrochloride), some of which are listed below:
Chemical synthesis method:
It can be prepared by reacting the precursor compound dichloroisopropanamide with N-ethyl-2-amino-5-chlorobenzoic acid. Concrete reaction process is: at first dichloroisopropanamide and N-ethyl-2-amino-5-chlorobenzoic acid are reacted under the presence of immobilized ammonium carbonate, obtain deschloro-N-ethyl-Ketamine; Then it is mixed with Hydrochloric acid reaction to obtain product.
Before discussing the use of Deschloro-N-ethyl-Ketamine (hydrochloride), it must be clearly stated that such compounds may belong to strictly regulated substances, and their research and application must comply with international and domestic laws and regulations. This content aims to explore the possible fields involved in such compounds from the perspective of scientific research and legal applications, rather than encouraging or supporting illegal activities.
Drug chemistry research: As part of drug chemistry research, dechlorinated N-ethylketamine (hydrochloride) may be used to explore the design and synthesis of novel drug molecules. This type of research helps to enhance the understanding of the mechanisms of drug action and may provide important clues for the development of new drugs.
Neuroscience research: As this compound may be related to the central nervous system, neuroscientists may be interested in it. By studying the effects of this compound on neurotransmitters, receptors, or ion channels, we can enhance our understanding of nervous system function and potentially provide new strategies for treating neurological diseases.
Toxicological research: Given the potential toxicity of this compound, toxicologists may conduct in-depth research on it. By evaluating the toxic effects, dose-response relationships, and long-term exposure effects of this compound on organisms, scientific basis can be provided for the development of safety standards and preventive measures.
Drug precursors: In some cases, dechlorinated N-ethylketamine (hydrochloride) may be used as a raw material for the synthesis of other drugs or drug precursors. These drugs may be used to treat various diseases, such as mental illness, neurological disorders, or pain. However, this application must comply with strict regulations and guiding principles to ensure the safety and effectiveness of the final product.
Tool compounds in scientific research: In fields such as neuroscience, pharmacology, and toxicology, this compound may be used as a tool compound. By observing and analyzing the impact of this compound on biological or cellular models, scientists can better understand the mechanisms of specific biological processes or diseases.
Education and training: In higher education and vocational training, dechlorinated N-ethylketamine (hydrochloride) may be used as a teaching material. By exposing and analyzing these compounds, students can deepen their understanding of fields such as chemistry, biology, and pharmacology. However, this use must be carried out under appropriate regulatory and safety measures.
It must be emphasized that the research and application of dechlorinated N-ethylketamine (hydrochloride) must comply with international and domestic laws and regulations. Any activity involving this compound must be based on scientific research and legal application. At the same time, we must also recognize the important responsibility that scientists and researchers undertake in promoting technological progress and enhancing human well-being. By adhering to legal and ethical standards, we can ensure that the research and application of such compounds can have a positive impact on humanity.
Deschloro-N-ethyl-Ketamine (hydrochloride) is a drug belonging to the Fenoxydiisoxazole-isopropylamine class of compounds. Here are some of its chemical reaction properties:
1. Carboxylic acid derivative reaction:
There is a hydrogen atom on the methylene position in dichloro-N-ethyl-Ketamine (hydrochloride), which can undergo carboxylic acid derivatization reactions through acylation and esterification reactions. For example, acylation reagents such as propionyl chloride or acetyl chloride can be used to react with them to obtain corresponding acylation products.
Esterification reaction:
Esterification reaction is one of the most common derivative reactions of carboxylic acids, which usually involves the condensation reaction between carboxyl groups and alcohols or phenols to produce esters and water. In this reaction, the carboxyl group in the carboxylic acid undergoes acid-base neutralization with the hydroxyl group in the alcohol or phenol, generating water and forming an ester molecule. This reaction usually requires the presence of acidic catalysts, such as sulfuric acid or superphosphate.
Acyl chloride reaction:
Acyl chloride reaction is the reaction between carboxyl groups in carboxylic acids and chlorides to produce acyl chloride. This reaction typically uses thiol chloride (SOCl2) as a chlorinating agent to generate acyl chloride, sulfur dioxide, and hydrochloric acid. Acyl chloride is an important organic synthesis intermediate that can be used to prepare other carboxylic acid derivatives.
Acyl bromide reaction:
Acyl bromide reaction is similar to acyl chloride reaction, which is a reaction between carboxyl groups in carboxylic acids and bromide to generate acyl bromide.
2. Nucleophilic substitution:
Deschro-N-ethyl-Ketamine (hydrochloride) can undergo nucleophilic substitution. For example, it can react with sodium thioacetate (NaSEt) under alkaline conditions to generate corresponding thioalcohol products.
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