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CAS 190190-47-7

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Boc-(S)-3-amino-4-(2-thienyl)-butyric acid

Description:
Boc-(S)-3-amino-4-(2-thienyl)-butyric acid is a chemical compound characterized by its structure, which includes a butyric acid backbone with an amino group and a thienyl substituent. The "Boc" (tert-butyloxycarbonyl) group serves as a protecting group for the amino functionality, making it useful in peptide synthesis and other organic reactions. The presence of the thienyl group introduces aromatic characteristics and can influence the compound's biological activity and solubility. This compound is typically utilized in medicinal chemistry and research, particularly in the development of pharmaceuticals due to its potential as an amino acid derivative. Its stereochemistry, indicated by the "(S)" designation, suggests that it exists as one specific enantiomer, which can be crucial for biological activity. The compound's properties, such as solubility, melting point, and reactivity, are influenced by its functional groups and overall molecular structure, making it a subject of interest in various chemical and biological studies.
Formula:C13H19NO4S
InChI:InChI=1/C13H19NO4S/c1-13(2,3)18-12(17)14-9(8-11(15)16)7-10-5-4-6-19-10/h4-6,9H,7-8H2,1-3H3,(H,14,17)(H,15,16)/t9-/m1/s1
SMILES:CC(C)(C)OC(=N[C@H](Cc1cccs1)CC(=O)O)O
Synonyms:
  • (3S)-3-[(tert-butoxycarbonyl)amino]-4-thiophen-2-ylbutanoic acid
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