The chemical substance known as (4R)-4-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}-5-phenylpentanoic acid, with the CAS number 269078-74-2, is a synthetic amino acid derivative. This compound features a chiral center at the fourth carbon, contributing to its specific stereochemistry, which is crucial for its biological activity. The presence of the fluorenylmethoxycarbonyl (Fmoc) group indicates that it is likely used in peptide synthesis as a protective group for the amino functionality, facilitating the formation of peptide bonds while preventing unwanted reactions. The phenyl group attached to the pentanoic acid backbone enhances the compound's hydrophobic characteristics, which can influence its solubility and interaction with biological membranes. Additionally, the carboxylic acid functional group provides acidic properties, allowing for potential interactions in biochemical environments. Overall, this compound is significant in the field of medicinal chemistry and peptide synthesis, where its structural features can be exploited for the development of novel therapeutic agents.

(4R)-4-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}-5-phenylpentanoic acid

269078-74-2: (R)-4-(Fmoc-Amino)-5-Phenylpentanoic Acid

(R)-4-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-5-phenylpentanoic acid

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CAS 269078-74-2: (4R)-4-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}-5-phenylpentanoic acid

(R)-4-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-5-phenylpentanoic acid

Ref: 10-F623841

Fmoc-(R)-4-amino-5-phenylpentanoic acid

Ref: 3D-FF49150

(R)-4-((((9H-Fluoren-9-Yl)Methoxy)Carbonyl)Amino)-5-Phenylpentanoic Acid

Ref: 54-OR1025601

(R)-4-(Fmoc-amino)-5-phenylpentanoic acid

Ref: IN-DA003C9X

(R)-4-(Fmoc-amino)-5-phenylpentanoic acid

Ref: 7W-GM1964