Boronic acid, (2-ethylbutyl)-, with the CAS number 140614-19-3, is an organoboron compound characterized by the presence of a boron atom bonded to a hydroxyl group and an alkyl chain. This compound typically features a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols, making it valuable in various chemical applications, particularly in organic synthesis and materials science. The (2-ethylbutyl) group contributes to its hydrophobic characteristics, influencing its solubility and reactivity in different solvents. Boronic acids are often utilized in Suzuki coupling reactions, a key method for forming carbon-carbon bonds in the synthesis of complex organic molecules. Additionally, they can serve as intermediates in the production of pharmaceuticals and agrochemicals. The stability of boronic acids can vary based on their substituents, and they may exhibit unique properties such as pH sensitivity, which can be exploited in sensor technology and drug delivery systems. Overall, (2-ethylbutyl) boronic acid is a versatile compound with significant implications in both research and industrial applications.

Boronic acid, (2-ethylbutyl)-

140614-19-3: Boronic acid, (2-ethylbutyl)-, with the CAS number 140614-19-3, is an organoboron compound characterized by the presence of a boron atom bonded to a hydroxyl group and an alkyl chain. This compound typically features a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols, making it valuable in various chemical applications, particularly in organic synthesis and materials science. The (2-ethylbutyl) group contributes to its hydrophobic characteristics, influencing its solubility and reactivity in different solvents. Boronic acids are often utilized in Suzuki coupling reactions, a key method for forming carbon-carbon bonds in the synthesis of complex organic molecules. Additionally, they can serve as intermediates in the production of pharmaceuticals and agrochemicals. The stability of boronic acids can vary based on their substituents, and they may exhibit unique properties such as pH sensitivity, which can be exploited in sensor technology and drug delivery systems. Overall, (2-ethylbutyl) boronic acid is a versatile compound with significant implications in both research and industrial applications.

CAS 140614-19-3

Boronic acid, (2-ethylbutyl)-

(2-Ethylbutyl)boronic acid

Ref: IN-DA001CK7

(2-Ethylbutyl)boronic acid

Ref: 3D-QFA61419