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CAS 193001-91-1

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2-Chloro-6-methoxy-4-pyridinemethanol

Description:
2-Chloro-6-methoxy-4-pyridinemethanol is an organic compound characterized by its pyridine ring structure, which is substituted with a chlorine atom and a methoxy group, along with a hydroxymethyl group. The presence of the chlorine atom at the 2-position and the methoxy group at the 6-position contributes to its unique reactivity and potential biological activity. This compound is typically a white to off-white solid and is soluble in polar solvents due to the hydroxymethyl group, which can engage in hydrogen bonding. Its molecular structure suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, as pyridine derivatives are often associated with various biological activities. The compound may exhibit properties such as antimicrobial or anti-inflammatory effects, although specific biological data would depend on empirical studies. Safety data should be consulted for handling and usage, as halogenated compounds can pose health risks. Overall, 2-Chloro-6-methoxy-4-pyridinemethanol represents a versatile structure in organic synthesis and drug development.
Formula:C7H8ClNO2
InChI:InChI=1S/C7H8ClNO2/c1-11-7-3-5(4-10)2-6(8)9-7/h2-3,10H,4H2,1H3
InChI key:InChIKey=LGAAPDVGNCACDI-UHFFFAOYSA-N
SMILES:C(O)C=1C=C(OC)N=C(Cl)C1
Synonyms:
  • (2-Chloro-6-methoxypyridin-4-yl)methanol
  • 2-Chloro-6-methoxy-4-pyridinemethanol
  • 4-Pyridinemethanol, 2-chloro-6-methoxy-
  • [2-Chloro-6-(methyloxy)-4-pyridinyl]methanol
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