The chemical substance known as (βR)-β-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-4-fluorobenzenebutanoic acid, with the CAS number 331763-70-3, is a synthetic compound primarily utilized in the field of medicinal chemistry and peptide synthesis. It features a fluorinated aromatic ring, which contributes to its unique electronic properties and potential biological activity. The presence of the fluorenylmethoxycarbonyl (Fmoc) group indicates its application as a protecting group for amino acids during peptide synthesis, allowing for selective deprotection under specific conditions. The compound's structure includes a butanoic acid moiety, which may influence its solubility and interaction with biological systems. Additionally, the chirality at the β position suggests that it may exhibit stereospecific interactions, which can be critical for its efficacy in biological applications. Overall, this compound represents a versatile building block in the development of pharmaceuticals and biologically active molecules, with potential implications in drug design and therapeutic applications.

(βR)-β-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-4-fluorobenzenebutanoic acid

331763-70-3: (R)-Fmoc-4-Fluoro-Beta-Homophe-Oh, (βR)-β-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-4-fluorobenzenebutanoic acid, Benzenebutanoic acid, β-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-4-fluoro-, (βR)-, H-D-β-HoPhe(4-F)-OH.HCl

Fmoc-(R)-3-Amino-4-(4-fluorophenyl)-butyric acid

(R)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(4-fluorophenyl)butanoic acid

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CAS 331763-70-3: (βR)-β-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-4-fluorobenzenebutanoic acid

Fmoc-(R)-3-Amino-4-(4-fluorophenyl)-butyric acid

Ref: 54-PC101097

(R)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(4-fluorophenyl)butanoic acid

Ref: IN-DA003CBA

Fmoc-4-fluoro-D-β-homophenylalanine

Ref: 3D-FF50239

(R)-Fmoc-4-fluoro-β-Homophe-OH

Ref: 7W-GM4612

Fmoc-(R)-3-Amino-4-(4-fluorophenyl)-butyric acid

Ref: 10-F603414