B-(3-Bromo-5-butoxyphenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is substituted with a bromine atom and a butoxy group. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible complexes with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The bromine substituent can enhance the reactivity of the phenyl ring, facilitating electrophilic aromatic substitution reactions. The butoxy group contributes to the compound's solubility in organic solvents and may influence its biological activity. Additionally, boronic acids are known for their role in Suzuki coupling reactions, a key method for forming carbon-carbon bonds in the synthesis of complex organic molecules. Overall, B-(3-Bromo-5-butoxyphenyl)boronic acid is a versatile compound with potential applications in pharmaceuticals and materials science, owing to its unique structural features and reactivity.

B-(3-Bromo-5-butoxyphenyl)boronic acid

1072951-84-8: (3-Bromo-5-butoxyphenyl)boronic acid, Boronic acid, B-(3-bromo-5-butoxyphenyl)-, 3-Bromo-5-butoxyphenylboronic acid, B-(3-Bromo-5-butoxyphenyl)boronic acid

(3-Bromo-5-butoxyphenyl)boronic acid

3-BROMO-5-BUTOXYPHENYLBORONIC ACID

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CAS 1072951-84-8: B-(3-Bromo-5-butoxyphenyl)boronic acid

(3-Bromo-5-butoxyphenyl)boronic acid

Ref: 10-F212588

3-BROMO-5-BUTOXYPHENYLBORONIC ACID

Ref: IN-DA003BRB

3-Bromo-5-butoxyphenylboronic acid

Ref: 3D-XSB95184

3-Bromo-5-butoxyphenylboronic acid

Ref: 54-OR360359