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CAS 866629-21-2

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6-Chloro-α-methyl-3-pyridineacetic acid

Description:
6-Chloro-α-methyl-3-pyridineacetic acid is a chemical compound characterized by its pyridine ring structure, which is a six-membered aromatic ring containing one nitrogen atom. The presence of a chlorine atom at the 6-position and a methyl group at the α-position contributes to its unique reactivity and properties. This compound typically exhibits acidic behavior due to the carboxylic acid functional group, allowing it to participate in various chemical reactions, including esterification and amidation. Its molecular structure suggests potential applications in pharmaceuticals, particularly in the development of drugs targeting neurological or metabolic pathways, given the pyridine moiety's prevalence in biologically active compounds. Additionally, the chlorine substituent may enhance lipophilicity, influencing the compound's bioavailability and pharmacokinetics. As with many pyridine derivatives, it may also exhibit specific interactions with biological targets, making it of interest in medicinal chemistry. Safety and handling precautions should be observed, as with all chemical substances, due to potential toxicity or reactivity.
Formula:C8H8ClNO2
InChI:InChI=1S/C8H8ClNO2/c1-5(8(11)12)6-2-3-7(9)10-4-6/h2-5H,1H3,(H,11,12)
InChI key:InChIKey=DRPAFECWIBKIAL-UHFFFAOYSA-N
SMILES:C(C(O)=O)(C)C=1C=CC(Cl)=NC1
Synonyms:
  • 2-(6-Chloropyridin-3-yl)propanoic acid
  • 6-Chloro-α-methyl-3-pyridineacetic acid
  • 3-Pyridineacetic acid, 6-chloro-α-methyl-
  • 2-(2-Chloro-5-pyridinyl)propionic acid
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