CAS 1228542-64-0

(S)-2-(tert-butoxycarbonylaMino)-2-(3-fluorophenyl)acetic acid

Description:

(S)-2-(tert-butoxycarbonylamino)-2-(3-fluorophenyl)acetic acid is a chiral amino acid derivative characterized by its specific stereochemistry and functional groups. The presence of a tert-butoxycarbonyl (Boc) group indicates that it is a protected amino acid, commonly used in peptide synthesis to prevent unwanted reactions at the amino group. The molecule features a fluorophenyl group, which can influence its biological activity and lipophilicity due to the electronegative fluorine atom. This compound is likely to exhibit properties typical of amino acids, such as solubility in polar solvents and the ability to participate in hydrogen bonding. Its chiral nature suggests that it may have specific interactions with biological targets, making it of interest in pharmaceutical applications. Additionally, the presence of the carboxylic acid functional group contributes to its acidity and potential reactivity in various chemical reactions. Overall, this compound's unique structure and functional groups make it a valuable candidate for further research in medicinal chemistry and drug development.

Formula: C₁₃H₁₆FNO₄

Synonyms:

• N-Boc-S-3-FluoroPhenylglycine
• (S)-2-(tert-butoxycarbonylaMino)-2-(3-fluorophenyl)acetic acid
• Benzeneacetic acid, α-[[(1,1-dimethylethoxy)carbonyl]amino]-3-fluoro-, (αS)-
• Boc-(S)-aMino-(3-fluorophenyl)acetic acid

(S)-2-((tert-butoxycarbonyl)amino)-2-(3-fluorophenyl)acetic acid

CAS: 1228542-64-0

Purity: 97%

Molecular weight: 269.2720032

Ref: 10-F777252

(2S)-2-[(tert-Butoxy)carbonylamino]-2-(3-fluorophenyl)acetic acid

CAS: 1228542-64-0

Versatile small molecule scaffold

Formula: C₁₃H₁₆FNO₄

Purity: Min. 95%

Molecular weight: 269.27 g/mol

Ref: 3D-DZB54264