CAS 1256358-73-2
:3-(3-chlorophenoxymethyl)phenylboronic acid
Description:
3-(3-Chlorophenoxymethyl)phenylboronic 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, including organic synthesis and medicinal chemistry. This compound features a phenyl ring substituted with a chlorophenyl group and a phenoxymethyl moiety, contributing to its structural complexity and potential reactivity. The presence of the boronic acid group allows for participation in Suzuki coupling reactions, which are pivotal in the formation of carbon-carbon bonds. Additionally, the chlorophenyl substituent may influence the compound's electronic properties and solubility, affecting its reactivity and interaction with biological targets. Overall, 3-(3-chlorophenoxymethyl)phenylboronic acid is a versatile compound with applications in drug discovery and materials science, particularly in the development of boron-containing pharmaceuticals and catalysts. Its unique structural features make it a subject of interest in ongoing research within the field of organic chemistry.
Formula:C13H12BClO3
Synonyms:- Boronic acid, B-[3-[(3-chlorophenoxy)methyl]phenyl]-
- 3-(3-chlorophenoxymethyl)phenylboronic acid
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