
CAS 2096339-93-2
:5-chloro-2,3-dimethoxypyridine-4-boronic acid
Description:
5-Chloro-2,3-dimethoxypyridine-4-boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a pyridine ring. This compound features a chlorine atom and two methoxy groups at the 2 and 3 positions of the pyridine, contributing to its unique reactivity and solubility properties. The boronic acid moiety is known for its ability to form reversible covalent bonds with diols, making it valuable in various applications, including organic synthesis and medicinal chemistry. The presence of the chlorine atom can influence the electronic properties of the molecule, potentially enhancing its reactivity in cross-coupling reactions. Additionally, the methoxy groups can affect the compound's polarity and solubility in organic solvents. Overall, 5-chloro-2,3-dimethoxypyridine-4-boronic acid is a versatile compound with potential applications in drug development and materials science, particularly in the synthesis of complex organic molecules through Suzuki coupling reactions.
Formula:C7H9BClNO4
Synonyms:- (5-Chloro-2,3-dimethoxypyridin-4-yl)boronic acid
- 5-chloro-2,3-dimethoxypyridine-4-boronic acid
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Found 3 products.
5-Chloro-2,3-dimethoxypyridine-4-boronic acid
CAS:Formula:C7H9BClNO4Purity:97%Color and Shape:SolidMolecular weight:217.41475-Chloro-2,3-dimethoxypyridine-4-boronic acid
CAS:5-Chloro-2,3-dimethoxypyridine-4-boronic acidPurity:97%Molecular weight:217.41g/mol


