Boronic acid, specifically B-[(1E)-4-hydroxy-1-buten-1-yl]- (CAS 916673-48-8), is an organoboron compound characterized by the presence of a boron atom bonded to a hydroxyl group and an alkene moiety. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The presence of the 4-hydroxy-1-buten-1-yl group suggests that it may participate in reactions typical of alkenes, such as electrophilic addition. Additionally, boronic acids are known for their role in Suzuki coupling reactions, which are vital in the formation of carbon-carbon bonds. The compound's structure may also impart specific reactivity and selectivity in chemical transformations, making it a valuable intermediate in the synthesis of more complex molecules. Overall, this boronic acid derivative is significant in both academic research and industrial applications due to its unique chemical properties.

Boronic acid, B-[(1E)-4-hydroxy-1-buten-1-yl]-

916673-48-8: Boronic acid, specifically B-[(1E)-4-hydroxy-1-buten-1-yl]- (CAS 916673-48-8), is an organoboron compound characterized by the presence of a boron atom bonded to a hydroxyl group and an alkene moiety. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The presence of the 4-hydroxy-1-buten-1-yl group suggests that it may participate in reactions typical of alkenes, such as electrophilic addition. Additionally, boronic acids are known for their role in Suzuki coupling reactions, which are vital in the formation of carbon-carbon bonds. The compound's structure may also impart specific reactivity and selectivity in chemical transformations, making it a valuable intermediate in the synthesis of more complex molecules. Overall, this boronic acid derivative is significant in both academic research and industrial applications due to its unique chemical properties.

CAS 916673-48-8

Boronic acid, B-[(1E)-4-hydroxy-1-buten-1-yl]-

(E)-(4-Hydroxybut-1-en-1-yl)boronic acid

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