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CAS 154593-58-5

:

(αS)-α-Amino-5-bromo-2-thiophenepropanoic acid

Description:
(αS)-α-Amino-5-bromo-2-thiophenepropanoic acid, with the CAS number 154593-58-5, is an amino acid derivative characterized by the presence of a bromine atom and a thiophene ring in its structure. This compound features a chiral center, which contributes to its stereochemical properties, specifically the (αS) configuration. The thiophene moiety imparts unique electronic and steric characteristics, making it of interest in various chemical and biological applications. The presence of the amino group (-NH2) indicates that it can participate in typical amino acid reactions, such as peptide bond formation. Additionally, the bromine substituent can enhance reactivity and facilitate further chemical modifications. This compound may exhibit biological activity, potentially influencing neurotransmitter systems or serving as a building block in pharmaceutical synthesis. Its solubility, stability, and reactivity can vary depending on the pH and solvent conditions, which are important considerations for its practical applications in research and industry.
Formula:C7H8BrNO2S
InChI:InChI=1S/C7H8BrNO2S/c8-6-2-1-4(12-6)3-5(9)7(10)11/h1-2,5H,3,9H2,(H,10,11)/t5-/m0/s1
InChI key:InChIKey=LKORPMMOJAJYLC-YFKPBYRVSA-N
SMILES:C([C@@H](C(O)=O)N)C1=CC=C(Br)S1
Synonyms:
  • (2S)-2-Amino-3-(5-bromo-2-thienyl)propanoic acid
  • (2S)-2-Amino-3-(5-bromothiophen-2-yl)propanoic acid
  • (2S)-2-Amino-3-(5-bromothiophen-2-yl)propionic acid
  • (2S)-Amino-3-(5-bromothiophen-2-yl)propionic acid
  • (S)-2-Amino-3-(5-bromothiophen-2-yl)propanoic acid
  • (S)-2-Amino-3-(5-bromothiophen-2-yl)propanoicacid
  • (αS)-α-Amino-5-bromo-2-thiophenepropanoic acid
  • 2-Thiophenepropanoic acid, α-amino-5-bromo-, (S)-
  • 2-Thiophenepropanoic acid, α-amino-5-bromo-, (αS)-
  • 3-(5-Bromothien-2-yl)-L-alanine
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