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CAS 1231709-27-5

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(2S)-2-Amino-2-methyl-4-pentynoic acid

Description:
(2S)-2-Amino-2-methyl-4-pentynoic acid, also known as a derivative of amino acids, is characterized by its unique structure that includes an alkyne functional group. This compound features a chiral center at the second carbon, which contributes to its stereochemistry, specifically the S configuration. The presence of both an amino group and a carboxylic acid group makes it an α-amino acid, allowing it to participate in various biochemical processes. Its alkyne moiety can engage in reactions typical of unsaturated compounds, such as addition reactions. This compound is of interest in synthetic organic chemistry and may have applications in the development of pharmaceuticals or as a building block in peptide synthesis. Additionally, its properties, such as solubility and reactivity, can be influenced by the presence of the alkyne and the amino acid functional groups, making it a versatile compound in research and industrial applications.
Formula:C6H9NO2
InChI:InChI=1S/C6H9NO2/c1-3-4-6(2,7)5(8)9/h1H,4,7H2,2H3,(H,8,9)/t6-/m0/s1
InChI key:InChIKey=FSBNDYYRTZBHAN-LURJTMIESA-N
SMILES:[C@](CC#C)(C(O)=O)(C)N
Synonyms:
  • (2S)-2-Amino-2-methyl-4-pentynoic acid
  • (S)-2-Amino-2-methylpent-4-ynoic acid
  • 4-Pentynoic acid, 2-amino-2-methyl-, (2S)-
  • Α-ME-GLY(PROPARGYL)-OH
  • (2S)-2-amino-2-methylpent-4-ynoic acid
  • α-methyl-D-Propargylglycine
  • (S)-Α-PROPARGYLALANINE
  • α-Me-Gly(Propargyl)-OH
  • Alpha-Methyl-Gly(Propargyl)-OH
  • (S)-2-Amino-2-methyl-4-pentynoic acid
  • Alpha-methyl-D-Propargylglycine
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