CAS 219945-56-9: 4-(Isopropylamino)benzeneboronic acid

Description: 4-(Isopropylamino)benzeneboronic acid, with the CAS number 219945-56-9, is an organic compound that belongs to the class of boronic acids. It features a boronic acid functional group (-B(OH)2) attached to a benzene ring that is further substituted with an isopropylamino group. This compound is characterized by its ability to form reversible covalent bonds with diols, making it useful in various applications, including medicinal chemistry and materials science. The presence of the isopropylamino group enhances its solubility and reactivity, allowing it to participate in Suzuki-Miyaura cross-coupling reactions, which are pivotal in the synthesis of complex organic molecules. Additionally, the boronic acid moiety can act as a pH-sensitive group, which is beneficial in drug delivery systems. Overall, 4-(Isopropylamino)benzeneboronic acid is a versatile compound with significant implications in synthetic organic chemistry and pharmaceutical development.

Formula: C₉H₁₄BNO₂

InChI: InChI=1/C9H14BNO2/c1-7(2)11-9-5-3-8(4-6-9)10(12)13/h3-7,11-13H,1-2H3

Synonyms:

• [4-(Isopropylamino)Phenyl]Boronic Acid

4-(Isopropylamino)phenylboronic acid

CAS: 219945-56-9

• Formula: C₉H₁₄BNO₂
• Molecular weight: 179.0240

(4-(Isopropylamino)phenyl)boronic acid

CAS: 219945-56-9

• Purity: 98+%
• Molecular weight: 179.02999877929688

4-(Isopropylamino)phenylboronic acid

CAS: 219945-56-9

Versatile small molecule scaffold

• Formula: C₉H₁₄BNO₂
• Purity: Min. 95%
• Molecular weight: 179.03 g/mol