The chemical substance known as (βS)-β-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-3-thiophenebutanoic acid, with the CAS number 270263-01-9, is a synthetic compound primarily used in the field of medicinal chemistry and peptide synthesis. It features a thiophene ring, which contributes to its unique electronic properties and potential biological activity. The presence of the fluorenylmethoxycarbonyl (Fmoc) group indicates that it is likely used as a protecting group for amino acids during peptide synthesis, facilitating the selective modification of amino acids without affecting other functional groups. The compound's structure suggests it may exhibit specific interactions with biological targets, making it of interest in drug development. Additionally, its stereochemistry, indicated by the (βS) designation, implies that it has a specific spatial arrangement that could influence its biological activity and interactions. Overall, this compound exemplifies the complexity and utility of synthetic organic molecules in pharmaceutical applications.

(βS)-β-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-3-thiophenebutanoic acid

270263-01-9: The chemical substance known as (βS)-β-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-3-thiophenebutanoic acid, with the CAS number 270263-01-9, is a synthetic compound primarily used in the field of medicinal chemistry and peptide synthesis. It features a thiophene ring, which contributes to its unique electronic properties and potential biological activity. The presence of the fluorenylmethoxycarbonyl (Fmoc) group indicates that it is likely used as a protecting group for amino acids during peptide synthesis, facilitating the selective modification of amino acids without affecting other functional groups. The compound's structure suggests it may exhibit specific interactions with biological targets, making it of interest in drug development. Additionally, its stereochemistry, indicated by the (βS) designation, implies that it has a specific spatial arrangement that could influence its biological activity and interactions. Overall, this compound exemplifies the complexity and utility of synthetic organic molecules in pharmaceutical applications.

CAS 270263-01-9

(βS)-β-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-3-thiophenebutanoic acid

(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(thiophen-3-yl)butanoic acid

Ref: IN-DA007M1J

Fmoc-(S)-3-Amino-4-(3-thienyl)-butyric acid

Ref: 10-F765130