CAS 218608-97-0: Boc-(S)-3-amino-4-(4-fluoro-phenyl)-butyric acid

Description: Boc-(S)-3-amino-4-(4-fluoro-phenyl)-butyric acid is a chemical compound characterized by its structure, which includes a tert-butyloxycarbonyl (Boc) protecting group, an amino group, and a fluoro-substituted phenyl moiety. This compound is typically used in peptide synthesis and medicinal chemistry due to its ability to serve as a building block for more complex molecules. The presence of the Boc group provides stability and protection to the amino group during synthetic procedures, allowing for selective reactions. The (S) configuration indicates that it is a chiral molecule, which is significant in biological systems where stereochemistry can influence activity and interactions. The 4-fluorophenyl group enhances the compound's lipophilicity and may influence its pharmacological properties. Overall, Boc-(S)-3-amino-4-(4-fluoro-phenyl)-butyric acid is notable for its utility in drug development and its role in the synthesis of biologically active compounds.

Formula: C₁₅H₂₀FNO₄

InChI: InChI=1/C15H20FNO4/c1-15(2,3)21-14(20)17-12(9-13(18)19)8-10-4-6-11(16)7-5-10/h4-7,12H,8-9H2,1-3H3,(H,17,20)(H,18,19)/t12-/m0/s1

Synonyms:

• (3S)-3-[(tert-butoxycarbonyl)amino]-4-(4-fluorophenyl)butanoic acid

Benzenebutanoic acid, b-[[(1,1-dimethylethoxy)carbonyl]amino]-4-fluoro-,(bS)-

CAS: 218608-97-0

• Formula: C₁₅H₂₀FNO₄
• Purity: 97%
• Color and Shape: Solid
• Molecular weight: 297.322

(S)-3-((tert-Butoxycarbonyl)amino)-4-(4-fluorophenyl)butanoic acid

CAS: 218608-97-0

• Purity: 95.0%
• Molecular weight: 297.32598876953125

Boc-b-HoPhe(4-F)-OH

CAS: 218608-97-0

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• Formula: C₁₅H₂₀FNO₄
• Purity: Min. 95%
• Molecular weight: 297.32 g/mol