The chemical substance known as (3R)-3-[(tert-butoxycarbonyl)amino]-4-[3-(trifluoromethyl)phenyl]butanoic acid, with the CAS number 269726-74-1, is an amino acid derivative characterized by its complex structure. It features a tert-butoxycarbonyl (Boc) protecting group, which is commonly used in peptide synthesis to protect the amino group during reactions. The presence of a trifluoromethyl group on the phenyl ring enhances the compound's lipophilicity and can influence its biological activity. This compound is typically utilized in pharmaceutical research and development, particularly in the synthesis of peptide-based drugs. Its chirality, indicated by the (3R) configuration, suggests that it may exhibit specific interactions in biological systems, making it of interest in medicinal chemistry. The carboxylic acid functional group contributes to its acidity and potential reactivity in various chemical reactions. Overall, this compound exemplifies the intricate design often found in drug development, combining structural features that may enhance efficacy and selectivity in therapeutic applications.

(3R)-3-[(tert-butoxycarbonyl)amino]-4-[3-(trifluoromethyl)phenyl]butanoic acid

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CAS 269726-74-1: (3R)-3-[(tert-butoxycarbonyl)amino]-4-[3-(trifluoromethyl)phenyl]butanoic acid

Boc-(R)-3-Amino-4-(3-Trifluoromethyl-Phenyl)-Butyric Acid

Ref: 3D-FB95258

(R)-3-((tert-Butoxycarbonyl)amino)-4-(3-(trifluoromethyl)phenyl)butanoic acid

Ref: 10-F695036

(R)-3-((tert-Butoxycarbonyl)amino)-4-(3-(trifluoromethyl)phenyl)butanoic acid

Ref: IN-DA003OEO