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CAS 332064-87-6

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(3R)-3-aminohex-5-ynoic acid hydrochloride

Description:
(3R)-3-aminohex-5-ynoic acid hydrochloride is an amino acid derivative characterized by its unique structure, which includes a terminal alkyne functional group and an amino group. This compound features a six-carbon backbone with a triple bond located between the fifth and sixth carbon atoms, contributing to its reactivity and potential applications in organic synthesis and medicinal chemistry. The presence of the amino group makes it a chiral molecule, with the (3R) designation indicating its specific stereochemistry. As a hydrochloride salt, it is typically more soluble in water than its free base form, enhancing its utility in biological and chemical applications. This compound may serve as a building block in the synthesis of peptides or other bioactive molecules, and its alkyne functionality can participate in various coupling reactions, such as the copper-catalyzed azide-alkyne cycloaddition (CuAAC). Overall, (3R)-3-aminohex-5-ynoic acid hydrochloride is a versatile compound with significant potential in both research and pharmaceutical development.
Formula:C6H10ClNO2
InChI:InChI=1/C6H9NO2.ClH/c1-2-3-5(7)4-6(8)9;/h1,5H,3-4,7H2,(H,8,9);1H/t5-;/m1./s1
SMILES:C#CC[C@H](CC(=O)O)N.Cl
Synonyms:
  • H-D-β-HoGly(Propargyl)-OH.HCl
  • (R)-3-Amino-5-Hexynoic Acid Hydrochloride
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