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CAS 83825-42-7

:

(S)-N-BOC-3-Thienylalanine

Description:
(S)-N-BOC-3-Thienylalanine is a synthetic amino acid derivative characterized by its unique thienyl group, which is a five-membered aromatic ring containing sulfur. This compound features a tert-butyloxycarbonyl (BOC) protecting group on the amino group, enhancing its stability and solubility in organic solvents, making it useful in peptide synthesis. The presence of the thienyl moiety contributes to its distinct electronic properties and potential biological activity, which may include interactions with various receptors or enzymes. As a chiral molecule, it exists in two enantiomeric forms, with the (S)-configuration being the biologically relevant form in many cases. This compound is often utilized in medicinal chemistry and peptide research due to its ability to incorporate into peptides while providing specific structural and functional characteristics. Its CAS number, 83825-42-7, allows for easy identification and reference in chemical databases. Overall, (S)-N-BOC-3-Thienylalanine serves as a valuable building block in the development of novel therapeutics and research applications.
Formula:C12H17NO4S
InChI:InChI=1/C12H17NO4S/c1-12(2,3)17-11(16)13-9(10(14)15)6-8-4-5-18-7-8/h4-5,7,9H,6H2,1-3H3,(H,13,16)(H,14,15)/t9-/m0/s1
SMILES:CC(C)(C)OC(=N[C@@H](Cc1ccsc1)C(=O)O)O
Synonyms:
  • N-tert-Butoxycarbonyl-3-thienyl-L-alanine
  • Boc-L-3-Thienylalanine-DCHA
  • (2S)-2-[(tert-butoxycarbonyl)amino]-3-thiophen-3-ylpropanoate
  • N-(tert-butoxycarbonyl)-3-thiophen-3-yl-L-alanine
  • Boc-L-3-(3-Thienyl)alanine
  • Boc-3-(3-Thienyl)-L-alanine
  • Boc-L-3-Thienylalanine Dcha Salt
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