CAS 167896-48-2

trans-3-Hydroxy-1-propenylboronic acid pinacol ester

Description:

Trans-3-Hydroxy-1-propenylboronic acid pinacol ester is an organoboron compound characterized by the presence of a boronic acid functional group and a pinacol ester moiety. This compound typically exhibits a clear, colorless to pale yellow appearance and is soluble in organic solvents such as dichloromethane and ethanol. It is known for its reactivity in various organic transformations, particularly in Suzuki-Miyaura cross-coupling reactions, which are pivotal in the synthesis of biaryl compounds. The presence of the hydroxyl group enhances its ability to form stable complexes with transition metals, making it a valuable intermediate in organic synthesis. Additionally, the trans configuration of the propenyl group contributes to its stereochemical properties, influencing its reactivity and interactions with other molecules. Due to its boronic acid functionality, it can also participate in the formation of boronate esters, which are useful in medicinal chemistry and materials science. Overall, trans-3-Hydroxy-1-propenylboronic acid pinacol ester is a versatile compound with significant applications in synthetic organic chemistry.

trans-3-Hydroxy-1-propenylboronic acid pinacol ester

CAS: 167896-48-2

Formula: C₉H₁₇BO₃

Purity: 98%

Color and Shape: Liquid

Molecular weight: 184.0405

Ref: IN-DA00B9X4

[(1E)-3-Hydroxyprop-1-en-1-yl]boronic acid, pinacol ester

CAS: 167896-48-2

[(1E)-3-Hydroxyprop-1-en-1-yl]boronic acid, pinacol ester

Purity: 97%

Color and Shape: Solid

Molecular weight: 184.04g/mol

Ref: 54-OR52076

(E)-3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)prop-2-en-1-ol

CAS: 167896-48-2

Purity: 98%

Molecular weight: 184.0399933

Ref: 10-F612356

(2E)-3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)prop-2-en-1-ol

CAS: 167896-48-2

Versatile small molecule scaffold

Formula: C₉H₁₇BO₃

Purity: Min. 95%

Molecular weight: 184.04 g/mol

Ref: 3D-SGA89648