CAS 1429510-64-4
:(2-Methoxy-3,5-dimethylpyridin-4-yl)boronic acid
Description:
(2-Methoxy-3,5-dimethylpyridin-4-yl)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 methoxy group and two methyl substituents on the pyridine, which influence its reactivity and solubility. 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 methoxy and methyl groups can enhance the compound's lipophilicity and may affect its biological activity. Typically, boronic acids are utilized in Suzuki coupling reactions, which are essential for forming carbon-carbon bonds in the synthesis of complex organic molecules. Additionally, this compound may exhibit properties such as moderate stability under ambient conditions, but it can be sensitive to moisture and air, necessitating careful handling and storage. Overall, (2-Methoxy-3,5-dimethylpyridin-4-yl)boronic acid is a versatile building block in synthetic chemistry.
Formula:C8H12BNO3
Synonyms:- Boronic acid, B-(2-methoxy-3,5-dimethyl-4-pyridinyl)-
- (2-Methoxy-3,5-dimethylpyridin-4-yl)boronic acid
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Found 2 products.
(2-Methoxy-3,5-dimethylpyridin-4-yl)boronic acid
CAS:<p>(2-Methoxy-3,5-dimethylpyridin-4-yl)boronic acid</p>Purity:98%Molecular weight:181g/mol
