CAS 218608-93-6: Boc-(R)-3-amino-4-(2-chloro-phenyl)-butyric acid

Description: Boc-(R)-3-amino-4-(2-chloro-phenyl)-butyric acid is a chemical compound characterized by its structure, which includes a butyric acid backbone with an amino group and a Boc (tert-butyloxycarbonyl) protecting group. The presence of the 2-chlorophenyl substituent introduces a halogen, which can influence the compound's reactivity and biological activity. This compound is typically used in peptide synthesis and medicinal chemistry due to its potential as a building block for more complex molecules. The Boc group serves as a protective moiety for the amino group, allowing for selective reactions without interfering with the amine functionality. The chirality at the 3-position (R configuration) is significant for biological activity, as it can affect the compound's interaction with biological targets. Overall, Boc-(R)-3-amino-4-(2-chloro-phenyl)-butyric acid is valued in research and development for its utility in synthesizing pharmaceuticals and studying structure-activity relationships in drug design.

Formula: C₁₅H₂₀ClNO₄

InChI: InChI=1/C15H20ClNO4/c1-15(2,3)21-14(20)17-11(9-13(18)19)8-10-6-4-5-7-12(10)16/h4-7,11H,8-9H2,1-3H3,(H,17,20)(H,18,19)/t11-/m1/s1

Synonyms:

• (3R)-3-[(tert-butoxycarbonyl)amino]-4-(2-chlorophenyl)butanoic acid
• Boc-D-β-HoPhe(2-Cl)-OH

(R)-N-Boc-3-Amino-4-(2-chlorophenyl)butanoic acid

CAS: 218608-93-6

• Formula: C₁₅H₂₀ClNO₄
• Purity: 98%
• Color and Shape: Solid
• Molecular weight: 313.7766

(R)-N-Boc-3-Amino-4-(2-chlorophenyl)butanoic acid

CAS: 218608-93-6

• Purity: 95.0%
• Molecular weight: 313.7799987792969

Boc-D-b-HoPhe(2-Cl)-OH

CAS: 218608-93-6

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• Formula: C₁₅H₂₀ClNO₄
• Purity: Min. 95%
• Molecular weight: 313.78 g/mol