CAS 1451392-23-6
:2-Chloro-5-methoxymethylphenylboronic acid
Description:
2-Chloro-5-methoxymethylphenylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, particularly in organic synthesis and medicinal chemistry. The compound features a chloro substituent and a methoxymethyl group on a phenyl ring, which can influence its reactivity and solubility. Typically, boronic acids are utilized in Suzuki coupling reactions, a key method for forming carbon-carbon bonds, and can also serve as intermediates in the synthesis of pharmaceuticals and agrochemicals. The presence of the chloro and methoxymethyl groups may enhance its reactivity or selectivity in specific reactions. Additionally, the compound's solubility in organic solvents and its stability under various conditions are important characteristics that determine its practical applications. Overall, 2-Chloro-5-methoxymethylphenylboronic acid is a versatile compound with significant utility in synthetic organic chemistry.
Formula:C8H10BClO3
Synonyms:- Boronic acid, B-[2-chloro-5-(methoxymethyl)phenyl]-
- 2-Chloro-5-methoxymethylphenylboronic acid
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