2-(Diisopropylcarbonyloxy)phenylboronic acid, with the CAS number 103681-98-7, is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring. This compound typically exhibits properties such as moderate solubility in organic solvents and limited solubility in water, which is common for many boronic acids. It is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The diisopropylcarbonyloxy group enhances its stability and reactivity, allowing for selective reactions in complex organic transformations. Additionally, boronic acids like this one are often utilized in Suzuki coupling reactions, a key method for forming carbon-carbon bonds in the synthesis of pharmaceuticals and agrochemicals. Overall, 2-(diisopropylcarbonyloxy)phenylboronic acid is a versatile compound with significant utility in both academic and industrial chemistry settings.

2-(DIISOPROPYLCARBANOYL) PHENYLBORONIC ACID

103681-98-7: Chembrdg-Bb 3200970, 2-[(Diisopropylamino)Carbonyl]Benzeneboronic Acid, Rarechem Ah Pb 0037, 2-(Diisopropylcarbamoyl)phenylboronic acid, 2-[(Diisopropylamino)carbonyl]phenylboronic acid, {2-[Bis(1-Methylethyl)Carbamoyl]Phenyl}Boronic Acid

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CAS 103681-98-7: 2-(DIISOPROPYLCARBANOYL) PHENYLBORONIC ACID

2-(DIISOPROPYLCARBANOYL) PHENYLBORONIC ACID

Ref: IN-DA008RR2

{2-[(Diisopropylamino)carbonyl]phenyl}boronic acid

Ref: 3D-FD121986

{2-[(diisopropylamino)carbonyl]phenyl}boronic acid

Ref: 10-F308004

2-(Diisopropylcarbanoyl) phenylboronic acid

Ref: TR-D493488