2-Furanpropanoic acid, α-amino-, (αS)-, also known by its CAS number 121786-31-0, is an organic compound characterized by the presence of both a furan ring and an amino acid structure. This compound features a furan moiety, which is a five-membered aromatic ring containing oxygen, contributing to its unique chemical properties. The α-amino group indicates that it possesses an amino functional group adjacent to the carboxylic acid, typical of amino acids, which allows for potential interactions in biological systems. The (αS)- designation refers to its specific stereochemistry, indicating that it has a particular spatial arrangement of atoms that can influence its biological activity and reactivity. This compound may exhibit properties such as solubility in polar solvents and potential reactivity with various electrophiles or nucleophiles due to the presence of both the carboxylic acid and amino groups. Its structural features suggest potential applications in pharmaceuticals, biochemistry, and materials science, particularly in the synthesis of biologically active molecules or as intermediates in organic synthesis.

2-Furanpropanoic acid, a-amino-, (aS)-

121786-31-0: 2-Furanpropanoic acid, α-amino-, (αS)-, also known by its CAS number 121786-31-0, is an organic compound characterized by the presence of both a furan ring and an amino acid structure. This compound features a furan moiety, which is a five-membered aromatic ring containing oxygen, contributing to its unique chemical properties. The α-amino group indicates that it possesses an amino functional group adjacent to the carboxylic acid, typical of amino acids, which allows for potential interactions in biological systems. The (αS)- designation refers to its specific stereochemistry, indicating that it has a particular spatial arrangement of atoms that can influence its biological activity and reactivity. This compound may exhibit properties such as solubility in polar solvents and potential reactivity with various electrophiles or nucleophiles due to the presence of both the carboxylic acid and amino groups. Its structural features suggest potential applications in pharmaceuticals, biochemistry, and materials science, particularly in the synthesis of biologically active molecules or as intermediates in organic synthesis.

CAS 121786-31-0

2-Furanpropanoic acid, a-amino-, (aS)-

2-Furanpropanoic acid, α-amino-, (αS)-

Ref: IN-DA00161I

(S)-2-Amino-3-(furan-2-yl)propanoic acid

Ref: 10-F224500

CAS 121786-31-0

2-Furanpropanoic acid, a-amino-, (aS)-

2-​Furanpropanoic acid, α-​amino-​, (αS)​-

Ref: IN-DA00161I

(S)-2-Amino-3-(furan-2-yl)propanoic acid

Ref: 10-F224500

2-Furanpropanoic acid, α-amino-, (αS)-