CAS 911482-75-2

Allylboronicacid neopentylester

Description:

Allylboronic acid neopentyl ester, with the CAS number 911482-75-2, is an organoboron compound characterized by the presence of both allyl and boronic acid functionalities. This compound typically exhibits a colorless to pale yellow liquid form and is known for its reactivity in various organic synthesis applications, particularly in the formation of carbon-carbon bonds through cross-coupling reactions. The boronic acid moiety allows for the formation of stable complexes with diols and other Lewis bases, making it useful in the development of boron-based reagents. Its neopentyl ester group contributes to its stability and solubility in organic solvents, enhancing its utility in synthetic chemistry. Additionally, allylboronic acid derivatives are often employed in the synthesis of pharmaceuticals and agrochemicals due to their ability to participate in nucleophilic addition reactions. Safety precautions should be observed when handling this compound, as organoboron compounds can be sensitive to moisture and air, potentially leading to hydrolysis or oxidation.

2-Allyl-5,5-dimethyl-1,3,2-dioxaborinane (stabilized with Phenothiazine)

CAS: 911482-75-2

Formula: C₈H₁₅BO₂

Purity: >98.0%(GC)(T)

Color and Shape: Colorless to Light yellow to Light orange clear liquid

Molecular weight: 154.02

Ref: 3B-A2574

2-Allyl-5,5-dimethyl-1,3,2-dioxaborinane

CAS: 911482-75-2

Formula: C₈H₁₇BO₃

Purity: 98%

Color and Shape: Liquid

Molecular weight: 172.0298

Ref: IN-DA00GXFQ

2-Allyl-5,5-Dimethyl-1,3,2-Dioxaborinane

CAS: 911482-75-2

2-Allyl-5,5-Dimethyl-1,3,2-Dioxaborinane

Purity: 98%

Molecular weight: 154.02g/mol

Ref: 54-OR1010248

2-Allyl-5,5-dimethyl-1,3,2-dioxaborinane

CAS: 911482-75-2

Purity: 98%+;RG

Molecular weight: 154.0200043

Ref: 10-F694001