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CAS 269726-89-8

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

Description:
Boc-(R)-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 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 properties, including potential biological activity. This compound is typically utilized in medicinal chemistry and drug development due to its structural features that may influence pharmacological interactions. Its chirality, indicated by the (R) configuration, is significant in determining its biological activity and interactions with biological targets. The compound is generally handled with standard laboratory safety precautions, and its stability and reactivity can vary based on environmental conditions and the presence of other reagents. Overall, Boc-(R)-3-amino-4-(2-thienyl)-butyric acid is a versatile intermediate in organic synthesis with potential applications in pharmaceuticals.
Formula:C13H19NO4S
InChI:InChI=1S/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-/m0/s1
InChI key:InChIKey=USQYZXFFROGLRS-VIFPVBQESA-N
SMILES:[C@@H](CC1=CC=CS1)(NC(OC(C)(C)C)=O)CC(O)=O
Synonyms:
  • (3R)-3-[(tert-butoxycarbonyl)amino]-4-thiophen-2-ylbutanoic acid
  • (βR)-β-[[(1,1-Dimethylethoxy)carbonyl]amino]-2-thiophenebutanoic acid
  • 2-Thiophenebutanoic acid, β-[[(1,1-dimethylethoxy)carbonyl]amino]-, (βR)-
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