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CAS 171670-23-8

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2-Pyridinecarboxylic acid, 6-(aminomethyl)-, methyl ester, hydrochloride (1:1)

Description:
2-Pyridinecarboxylic acid, 6-(aminomethyl)-, methyl ester, hydrochloride (1:1), commonly referred to as a pyridine derivative, exhibits several notable characteristics. This compound features a pyridine ring, which contributes to its aromatic properties and potential biological activity. The presence of the carboxylic acid and methyl ester functional groups suggests it may participate in various chemical reactions, including esterification and amidation. The aminomethyl group enhances its potential for forming hydrogen bonds, which can influence solubility and reactivity. As a hydrochloride salt, it is typically more soluble in water compared to its free base form, making it suitable for various applications in pharmaceuticals and organic synthesis. The compound may exhibit biological activity, potentially serving as a precursor or intermediate in the synthesis of more complex molecules. Its structural characteristics suggest it could interact with biological targets, making it of interest in medicinal chemistry. Overall, this compound's unique functional groups and structural features position it as a versatile entity in chemical research and development.
Formula:C8H10N2O2·ClH
InChI:InChI=1S/C8H10N2O2.ClH/c1-12-8(11)7-4-2-3-6(5-9)10-7;/h2-4H,5,9H2,1H3;1H
InChI key:InChIKey=QIDKZVAMKNKDAM-UHFFFAOYSA-N
SMILES:C(OC)(=O)C=1N=C(CN)C=CC1.Cl
Synonyms:
  • 2-Pyridinecarboxylic acid, 6-(aminomethyl)-, methyl ester, monohydrochloride
  • 2-Pyridinecarboxylic acid, 6-(aminomethyl)-, methyl ester, hydrochloride (1:1)
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