(R)-4-(BOC-AMINO)-5-phenylpentanoic acid is a chiral amino acid derivative characterized by its specific stereochemistry and functional groups. The "R" designation indicates the configuration around the chiral center, which influences its biological activity and interactions. The BOC (tert-butyloxycarbonyl) group serves as a protecting group for the amino functionality, making it useful in peptide synthesis and other organic reactions. This compound features a phenyl group, contributing to its hydrophobic characteristics and potential interactions in biological systems. The pentanoic acid backbone provides a five-carbon chain, which can affect the compound's solubility and reactivity. Overall, this substance is of interest in pharmaceutical chemistry, particularly in the development of peptide-based drugs and as a building block in organic synthesis. Its unique structure allows for specific interactions with biological targets, making it a valuable compound in medicinal chemistry research.

(R)-4-(BOC-AMINO)-5-PHENYLPENTANOIC ACID

195867-20-0: Boc-Γ-L-Dihomo-Phenylalanine

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

(R)-4-((tert-Butoxycarbonyl)amino)-5-phenylpentanoic acid

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CAS 195867-20-0: (R)-4-(BOC-AMINO)-5-PHENYLPENTANOIC ACID

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

Ref: 7W-GM2411

(R)-4-(BOC-AMINO)-5-PHENYLPENTANOIC ACID

Ref: IN-DA00746N

(R)-4-((tert-Butoxycarbonyl)amino)-5-phenylpentanoic acid

Ref: 10-F212992

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

Ref: 3D-FB49149