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CAS 270596-39-9

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Boc-(S)-3-amino-4-(3-chloro-phenyl)-butyric acid

Description:
Boc-(S)-3-amino-4-(3-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 3-chloro-phenyl substituent contributes to its unique properties, potentially influencing its biological activity and solubility. This compound is often utilized in peptide synthesis and medicinal chemistry due to its ability to serve as a building block for more complex molecules. The Boc group is commonly used to protect amines during chemical reactions, allowing for selective functionalization. The stereochemistry indicated by the (S) designation suggests that the compound has a specific spatial arrangement, which can be crucial for its interaction with biological targets. Overall, Boc-(S)-3-amino-4-(3-chloro-phenyl)-butyric acid is significant in research and development, particularly in the fields of pharmaceuticals and organic synthesis.
Formula:C15H20ClNO4
InChI:InChI=1/C15H20ClNO4/c1-15(2,3)21-14(20)17-12(9-13(18)19)8-10-5-4-6-11(16)7-10/h4-7,12H,8-9H2,1-3H3,(H,17,20)(H,18,19)/t12-/m0/s1
SMILES:CC(C)(C)OC(=N[C@@H](Cc1cccc(c1)Cl)CC(=O)O)O
Synonyms:
  • (3S)-3-[(tert-butoxycarbonyl)amino]-4-(3-chlorophenyl)butanoic acid
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