Product Name:Ethyl L-valinate hydrochloride

IUPAC Name:ethyl (2S)-2-amino-3-methylbutanoate hydrochloride

CAS:17609-47-1
Molecular Formula:C7H16ClNO2
Purity:98%
Catalog Number:CM119427
Molecular Weight:181.66

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Product Details

CAS NO:17609-47-1
Molecular Formula:C7H16ClNO2
Melting Point:-
Smiles Code:N[C@@H](C(C)C)C(OCC)=O.[H]Cl
Density:
Catalog Number:CM119427
Molecular Weight:181.66
Boiling Point:212.5°C at 760 mmHg
MDL No:MFCD00012511
Storage:Store at room temperature.

Category Infos

Amino Acids and Peptides
Amino acids are organic compounds containing a basic amino group and an acidic carboxyl group. Because amino acids contain both amino and carboxyl groups, they can be polymerized in an end-to-end manner, removing a molecule of water to form a covalent amide bond or peptide bond. Many amino acids are linked together end to end to form a polypeptide. Amino acids and peptides are important components in the fields of medicine and life sciences.
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Product Other Information

Product Overview Ethyl L-valinate hydrochloride, also known as ethyl L-valinate HCl, is an organic compound derived from the amino acid valine. It is a white, crystalline powder, soluble in water and insoluble in organic solvents. It is used in a variety of applications, including as a pharmaceutical intermediate, in chemical synthesis, and in laboratory experiments.
Synthesis and Application Ethyl L-valinate hydrochloride can be synthesized from the reaction of Ethyl L-valinate hydrochloride bromoacetate and L-valine, in the presence of a base such as sodium hydroxide or potassium hydroxide. The reaction is a nucleophilic substitution reaction, and yields Ethyl L-valinate hydrochloride L-valinate hydrochloride as the product. Ethyl L-valinate hydrochloride has a variety of scientific research applications. It has been used as a substrate for the enzyme transaminase, as a reagent for the synthesis of other compounds, and as a biochemical reagent in the study of protein-protein interactions. It has also been used in studies of the structure and function of enzymes, and in studies of the effects of drugs on cellular metabolism.
Future Directions Future research on Ethyl L-valinate hydrochloride L-valinate hydrochloride could focus on its mechanism of action and its biochemical and physiological effects. Additionally, further research could focus on its potential applications in drug development and its use as a pharmaceutical intermediate. Finally, further research could investigate its potential use in the development of new synthetic methods and its potential use as a reagent in chemical synthesis.