(S)-N-ethylalanine methyl ester is an amino acid derivative characterized by its chiral center, which imparts specific stereochemical properties. As an ester, it features a methyl group attached to the carboxylic acid functional group of alanine, while the ethyl group is linked to the amino group. This compound is typically a white to off-white solid or a viscous liquid, depending on its purity and environmental conditions. It is soluble in polar solvents such as water and alcohols, making it useful in various chemical applications, including peptide synthesis and as a building block in pharmaceuticals. The presence of the ethyl group enhances its lipophilicity compared to its parent amino acid, which can influence its biological activity and interaction with other molecules. Additionally, (S)-N-ethylalanine methyl ester can participate in various chemical reactions, including esterification and amidation, making it a versatile compound in organic synthesis. Its specific stereochemistry is crucial for its function in biological systems, particularly in the context of drug design and development.

(S)-N-ethylalanine Methyl ester

222550-60-9: (S)-N-ethylalanine methyl ester is an amino acid derivative characterized by its chiral center, which imparts specific stereochemical properties. As an ester, it features a methyl group attached to the carboxylic acid functional group of alanine, while the ethyl group is linked to the amino group. This compound is typically a white to off-white solid or a viscous liquid, depending on its purity and environmental conditions. It is soluble in polar solvents such as water and alcohols, making it useful in various chemical applications, including peptide synthesis and as a building block in pharmaceuticals. The presence of the ethyl group enhances its lipophilicity compared to its parent amino acid, which can influence its biological activity and interaction with other molecules. Additionally, (S)-N-ethylalanine methyl ester can participate in various chemical reactions, including esterification and amidation, making it a versatile compound in organic synthesis. Its specific stereochemistry is crucial for its function in biological systems, particularly in the context of drug design and development.

(S)-Methyl 2-(Ethylamino)-3-Methylbutanoate

CAS 222550-60-9

(S)-N-ethylalanine Methyl ester

(S)-N-ethylalanine Methyl ester

Ref: IN-DA00BHME

(S)-Methyl 2-(Ethylamino)-3-Methylbutanoate

Ref: 54-OR1008784

(S)-Methyl 2-(ethylamino)-3-methylbutanoate

Ref: 10-F224749