2-(2-Hydroxyethylamino)ethoxy-isopropyl-borinic acid, identified by its CAS number 119246-82-1, is a boronic acid derivative characterized by the presence of a boron atom bonded to an organic moiety that includes hydroxyethyl and ethoxy groups. 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 hydroxyethylamino group suggests potential for hydrogen bonding and increased solubility in polar solvents. Additionally, the isopropyl group may contribute to the compound's steric hindrance, influencing its reactivity and interactions with biological targets. Overall, this compound's unique structure allows it to participate in diverse chemical reactions, particularly in the context of drug development and materials science, where boronic acids are often utilized for their reactivity and ability to form complexes with biomolecules.

2-(2-hydroxyethylamino)ethoxy-isopropyl-borinic acid

119246-82-1: 2-(2-Hydroxyethylamino)ethoxy-isopropyl-borinic acid, identified by its CAS number 119246-82-1, is a boronic acid derivative characterized by the presence of a boron atom bonded to an organic moiety that includes hydroxyethyl and ethoxy groups. 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 hydroxyethylamino group suggests potential for hydrogen bonding and increased solubility in polar solvents. Additionally, the isopropyl group may contribute to the compound's steric hindrance, influencing its reactivity and interactions with biological targets. Overall, this compound's unique structure allows it to participate in diverse chemical reactions, particularly in the context of drug development and materials science, where boronic acids are often utilized for their reactivity and ability to form complexes with biomolecules.

CAS 119246-82-1

2-(2-hydroxyethylamino)ethoxy-isopropyl-borinic acid

4H-1,3,6,2-Dioxazaborocine, tetrahydro-2-(1-methylethyl)-

Ref: IN-DA000IG2