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CAS 1879026-29-5

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5-Chloro-2,6-dimethoxy-3-pyridinemethanol

Description:
5-Chloro-2,6-dimethoxy-3-pyridinemethanol is a chemical compound characterized by its pyridine ring structure, which is substituted with a chlorine atom and two methoxy groups at the 2 and 6 positions, along with a hydroxymethyl group at the 3 position. This compound typically exhibits properties associated with both aromatic and aliphatic functionalities, contributing to its potential reactivity and solubility in various solvents. The presence of the chlorine atom may impart specific electronic effects, influencing the compound's reactivity and interactions with biological systems. The methoxy groups can enhance lipophilicity, potentially affecting the compound's pharmacokinetic properties. As a pyridine derivative, it may exhibit biological activity, making it of interest in medicinal chemistry and drug development. Its molecular structure suggests potential applications in various fields, including agrochemicals and pharmaceuticals, although specific biological or chemical activities would require further investigation. Safety data and handling precautions should be considered, as with any chemical substance, to ensure proper usage and compliance with regulatory standards.
Formula:C8H10ClNO3
InChI:InChI=1S/C8H10ClNO3/c1-12-7-5(4-11)3-6(9)8(10-7)13-2/h3,11H,4H2,1-2H3
InChI key:InChIKey=UAOFMNLMJQAWGX-UHFFFAOYSA-N
SMILES:O(C)C1=C(CO)C=C(Cl)C(OC)=N1
Synonyms:
  • 5-Chloro-2,6-dimethoxy-3-pyridinemethanol
  • 3-Pyridinemethanol, 5-chloro-2,6-dimethoxy-
  • 5-Chloro-2,6-dimethoxypyridine-3-methanol
  • (5-chloro-2,6-dimethoxypyridin-3-yl)methanol
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