CAS 269726-92-3
:Boc-(R)-3-amino-4-(3-thienyl)-butyric acid
Description:
Boc-(R)-3-amino-4-(3-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 protective group for the amino functionality, making it useful in peptide synthesis and other organic reactions. The presence of the thienyl group, a five-membered aromatic ring containing sulfur, contributes to the compound's unique electronic and steric properties, potentially influencing its biological activity. This compound is typically utilized in medicinal chemistry and drug development, particularly in the design of compounds with potential therapeutic applications. Its chirality, indicated by the (R) configuration, is crucial for its biological interactions, as enantiomers can exhibit significantly different pharmacological effects. Overall, Boc-(R)-3-amino-4-(3-thienyl)-butyric acid is a versatile intermediate in organic synthesis, particularly in the context of developing novel pharmaceuticals.
Formula:C13H19NO4S
InChI:InChI=1/C13H19NO4S/c1-13(2,3)18-12(17)14-10(7-11(15)16)6-9-4-5-19-8-9/h4-5,8,10H,6-7H2,1-3H3,(H,14,17)(H,15,16)/t10-/m1/s1
SMILES:CC(C)(C)OC(=N[C@H](Cc1ccsc1)CC(=O)O)O
Synonyms:- (3R)-3-[(tert-butoxycarbonyl)amino]-4-thiophen-3-ylbutanoic acid
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