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CAS 190319-95-0

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(S)-N-BOC-2-(5-Bromothienyl)alanine

Description:
(S)-N-BOC-2-(5-Bromothienyl)alanine is a chemical compound characterized by its structure, which includes a thienyl group and a protected amino acid. The "N-BOC" designation indicates that the amine group is protected by a tert-butyloxycarbonyl (BOC) group, which is commonly used in peptide synthesis to prevent unwanted reactions. The presence of the 5-bromothienyl moiety introduces both a halogen and a heterocyclic aromatic system, which can influence the compound's reactivity and biological activity. This compound is typically utilized in organic synthesis and medicinal chemistry, particularly in the development of pharmaceuticals. Its chirality, denoted by the (S) configuration, suggests that it may exhibit specific interactions in biological systems, making it of interest in drug design. The CAS number 190319-95-0 uniquely identifies this compound, facilitating its recognition in chemical databases and literature. Overall, (S)-N-BOC-2-(5-Bromothienyl)alanine is a valuable intermediate in the synthesis of more complex molecules.
Formula:C12H15BrNO4S
InChI:InChI=1/C12H16BrNO4S/c1-12(2,3)18-11(17)14-8(10(15)16)6-7-4-5-9(13)19-7/h4-5,8H,6H2,1-3H3,(H,14,17)(H,15,16)/p-1/t8-/m0/s1
SMILES:CC(C)(C)OC(=N[C@@H](Cc1ccc(Br)s1)C(=O)[O-])O
Synonyms:
  • N-tert-Butoxycarbonyl-(5-bromo-2-thienyl)-L-alanine
  • 3-(5-bromothiophen-2-yl)-N-(tert-butoxycarbonyl)-L-alanine
  • (2S)-3-(5-bromothiophen-2-yl)-2-[(tert-butoxycarbonyl)amino]propanoate
  • Boc-L-2-(5-BromoThienyl)-alanine
  • Boc-3-(5-bromothien-2-yl)-L-alanine
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