B-(3-Butoxy-5-formylphenyl)boronic 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 and other nucleophiles. This compound features a phenyl ring substituted with a butoxy group and a formyl group, contributing to its reactivity and potential applications in organic synthesis and medicinal chemistry. The boronic acid moiety allows for participation in Suzuki-Miyaura cross-coupling reactions, making it valuable in the formation of carbon-carbon bonds. Additionally, the presence of the formyl group may facilitate further functionalization, enabling the synthesis of more complex molecules. The butoxy substituent enhances the solubility of the compound in organic solvents, which is advantageous for various chemical reactions. Overall, B-(3-Butoxy-5-formylphenyl)boronic acid is a versatile building block in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its unique structural features and reactivity profile make it a subject of interest in both academic and industrial research.

B-(3-Butoxy-5-formylphenyl)boronic acid

1072951-70-2: B-(3-Butoxy-5-formylphenyl)boronic acid, Boronic acid, B-(3-butoxy-5-formylphenyl)-

CAS 1072951-70-2: B-(3-Butoxy-5-formylphenyl)boronic acid

3-Butoxy-5-formylphenylboronic acid

Ref: 54-OR360828

3-BUTOXY-5-FORMYLPHENYLBORONIC ACID

Ref: IN-DA003BRN

(3-Butoxy-5-formylphenyl)boronic acid

Ref: 10-F691514