CAS 900174-62-1

Boronic acid, (4-chloro-3-ethoxyphenyl)-

Description:

Boronic acid, (4-chloro-3-ethoxyphenyl)-, identified by its CAS number 900174-62-1, is an organoboron compound characterized by the presence of a boronic acid functional group (-B(OH)2) attached to a phenyl ring that is substituted with a chloro group and an ethoxy group. This compound typically exhibits properties such as moderate solubility in polar solvents due to the presence of the boronic acid moiety, which can engage in hydrogen bonding. The chloro substituent can influence the compound's reactivity and electronic properties, while the ethoxy group may enhance solubility and steric effects. Boronic acids are known for their ability to form reversible complexes with diols, making them valuable in organic synthesis and materials science, particularly in the development of sensors and drug delivery systems. Additionally, the presence of the boron atom allows for unique reactivity patterns, including cross-coupling reactions, which are widely utilized in the synthesis of complex organic molecules.

Formula: C₈H₁₀BClO₃

AKOS BRN-1022

CAS: 900174-62-1

Formula: C₈H₁₀BClO₃

Purity: 97%

Color and Shape: Solid

Molecular weight: 200.4272

Ref: IN-DA00GTEF

4-Chloro-3-ethoxyphenylboronic acid

CAS: 900174-62-1

4-Chloro-3-ethoxyphenylboronic acid

Purity: 99%

Molecular weight: 200.43g/mol

Ref: 54-OR360931

(4-Chloro-3-ethoxyphenyl)boronic acid

CAS: 900174-62-1

Formula: C₈H₁₀BClO₃

Purity: 98%

Color and Shape: No data available.

Molecular weight: 200.43

Ref: 10-F215957