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CAS 93960-21-5

:

3-Pyridinepropanoic acid, α-amino-, hydrochloride (1:2), (αR)-

Description:
3-Pyridinepropanoic acid, α-amino-, hydrochloride (1:2), (αR)-, is a chemical compound characterized by its pyridine and amino acid structure. It features a pyridine ring attached to a propanoic acid moiety, which includes an amino group at the alpha position relative to the carboxylic acid. This compound is typically encountered as a hydrochloride salt, indicating the presence of hydrochloric acid in its formulation, which enhances its solubility in water. The (αR)- designation refers to the specific stereochemistry of the amino acid, indicating its chiral nature. This compound may exhibit biological activity, potentially acting as a neurotransmitter or influencing metabolic pathways due to its structural similarity to amino acids. Its properties include being hygroscopic and soluble in polar solvents, which is common for amino acids and their derivatives. As with many compounds containing both acidic and basic functional groups, it can participate in various chemical reactions, including peptide bond formation and other transformations relevant in organic synthesis and pharmaceutical applications.
Formula:C8H10N2O2·2ClH
InChI:InChI=1S/C8H10N2O2.2ClH/c9-7(8(11)12)4-6-2-1-3-10-5-6;;/h1-3,5,7H,4,9H2,(H,11,12);2*1H/t7-;;/m1../s1
InChI key:InChIKey=XORPRVNSFLBKBG-XCUBXKJBSA-N
SMILES:C([C@H](C(O)=O)N)C=1C=CC=NC1.Cl
Synonyms:
  • 3-Pyridinepropanoic acid, α-amino-, dihydrochloride, (R)-
  • 3-Pyridinepropanoic acid, α-amino-, hydrochloride (1:2), (αR)-
  • (R)-2-Amino-3-(pyridin-3-yl)propanoic acid dihydrochloride
  • 3-Pyridinepropanoic acid, α-amino-, dihydrochloride, (αR)-
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