CAS 66117-64-4

Borinic acid, bis(4-methylphenyl)-

Description:

Borinic acid, bis(4-methylphenyl)-, also known by its CAS number 66117-64-4, is an organoboron compound characterized by the presence of a boron atom bonded to two 4-methylphenyl groups and a hydroxyl group. This compound typically exhibits properties associated with boron compounds, such as Lewis acidity, which allows it to act as a catalyst in various organic reactions, particularly in the formation of carbon-carbon bonds. The presence of the methyl groups on the phenyl rings can influence its solubility and reactivity, making it more lipophilic compared to other boronic acids. Additionally, borinic acids are generally less stable than their boronic counterparts, often undergoing oxidation or hydrolysis under certain conditions. This compound may find applications in organic synthesis, materials science, and as a reagent in various chemical transformations. However, specific handling precautions should be observed due to potential reactivity and toxicity associated with organoboron compounds.

Formula: C₁₄H₁₅BO

BIS(4-TOLYL)BORONIC ACID

CAS: 66117-64-4

Formula: C₁₄H₁₅BO

Purity: 98%

Molecular weight: 210.0793

Ref: IN-DA00FFX1

Hydroxydi-p-tolylborane

CAS: 66117-64-4

Hydroxydi-p-tolylborane

Purity: ≥95%

Molecular weight: 210.08g/mol

Ref: 54-OR361247

Hydroxydi-p-tolylborane

Controlled Product

CAS: 66117-64-4

Applications Hydroxydi-p-tolylborane is a building block used as a reactant in the nickel-catalyzed cross-coupling of diarylborinic acids with aryl chlorides.
References Chen, X., et al.: ACS Catalys., 4, 379 (2014);

Formula: C₁₄H₁₅BO

Color and Shape: Neat

Molecular weight: 210.08

Ref: TR-H941753