CAS 331763-63-4

Benzenebutanoicacid, b-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-2-fluoro-, (bR)-

Description:

Benzenebutanoic acid, b-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-2-fluoro-, commonly referred to by its CAS number 331763-63-4, is a chemical compound that features a complex structure incorporating both aromatic and aliphatic components. This substance is characterized by the presence of a benzenebutanoic acid moiety, which contributes to its potential as a building block in organic synthesis. The fluorenylmethoxycarbonyl (Fmoc) group is notable for its use in protecting amino groups during peptide synthesis, indicating that this compound may play a role in the development of pharmaceuticals or biochemicals. The presence of a fluorine atom in the structure can enhance the compound's biological activity and lipophilicity, making it of interest in medicinal chemistry. Additionally, the stereochemistry indicated by the (bR) designation suggests that the compound exists in a specific chiral form, which can significantly influence its reactivity and interactions in biological systems. Overall, this compound exemplifies the intricate design often found in modern organic and medicinal chemistry.

Formula: C₂₅H₂₂FNO₄

Synonyms:

• Fmoc-(R)-3-Amino-4-(2-Fluoro-Phenyl)-Butyric Acid

Fmoc-(R)-3-Amino-4-(2-fluoro-phenyl)-butyric acid

CAS: 331763-63-4

Formula: C₂₅H₂₂FNO₄

Purity: 96%

Color and Shape: Solid

Molecular weight: 419.4449

Ref: IN-DA00BYZ9

Fmoc-(R)-3-Amino-4-(2-fluoro-phenyl)-butyric acid

CAS: 331763-63-4

Fmoc-(R)-3-Amino-4-(2-fluoro-phenyl)-butyric acid

Purity: 96%

Molecular weight: 419.44g/mol

Ref: 54-PC101319

Fmoc-(R)-3-Amino-4-(2-fluoro-phenyl)-butyric acid

CAS: 331763-63-4

Purity: 96%

Molecular weight: 419.4519958

Ref: 10-F609936