CAS 138500-85-3

(4-Bromomethylphenyl)boronic acid

Description:

(4-Bromomethylphenyl)boronic acid is an organoboron compound characterized by the presence of both a boronic acid functional group and a bromomethyl substituent on a phenyl ring. This compound typically appears as a white to off-white solid and is soluble in polar solvents such as water and alcohols, owing to the boronic acid group, which can form hydrogen bonds. The presence of the bromomethyl group enhances its reactivity, making it useful in various organic synthesis applications, particularly in cross-coupling reactions like Suzuki-Miyaura coupling, where it serves as a key intermediate for the formation of carbon-carbon bonds. Additionally, the boronic acid functionality allows for the formation of reversible complexes with diols, which is valuable in biological and medicinal chemistry contexts. Its reactivity and functional versatility make (4-Bromomethylphenyl)boronic acid a significant compound in the development of pharmaceuticals and agrochemicals. Safety precautions should be observed when handling this compound, as with many organoboron compounds, due to potential toxicity and reactivity.

Formula: C₁₃H₁₈BBrO₂

InChI: InChI=1/C13H18BBrO2/c1-12(2)13(3,4)17-14(16-12)11-7-5-10(9-15)6-8-11/h5-8H,9H2,1-4H3

SMILES: CC1(C)C(C)(C)OB(c2ccc(cc2)CBr)O1

Synonyms:

• 4-(Bromomethyl)phenylboronic acid pinacol cyclic ester~2-[(4-Bromomethyl)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
• 4-(Bromomethyl)benzeneboronic acid pinacol cyclic ester
• 2-[4-(Bromomethyl)Phenyl]-4,4,5,5-Tetramethyl-1,3,2-Dioxaborolane
• 4-(Bromomethyl)phenylboronic acid pinacol ester
• 4-(Bromomethyl)Benzeneboronic Acid Pinacol Ester

4-(Bromomethyl)benzeneboronic acid pinacol ester, 95%

CAS: 138500-85-3

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci

Formula: C₁₃H₁₈BBrO₂

Purity: 95%

Color and Shape: White to cream, Crystals or powder or crystalline powder

Molecular weight: 297.00

Ref: 02-L19954

1,3,2-Dioxaborolane, 2-[4-(bromomethyl)phenyl]-4,4,5,5-tetramethyl-

CAS: 138500-85-3

Formula: C₁₃H₁₈BBrO₂

Purity: 97%

Color and Shape: Solid

Molecular weight: 296.9958

Ref: IN-DA0019BQ

4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl Bromide

CAS: 138500-85-3

Formula: C₁₃H₁₈BBrO₂

Purity: >98.0%(GC)(T)

Color and Shape: White to Almost white powder to crystal

Molecular weight: 297.00

Ref: 3B-T2945

4-(Bromomethyl)benzeneboronic acid, pinacol ester

CAS: 138500-85-3

4-(Bromomethyl)benzeneboronic acid, pinacol ester

Purity: 98%

Molecular weight: 296.99581g/mol

Ref: 54-OR10381

2-(4-(Bromomethyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

CAS: 138500-85-3

Formula: C₁₃H₁₈BBrO₂

Purity: 97%

Color and Shape: Solid

Molecular weight: 297

Ref: 10-F092399

4-(Bromomethyl)benzeneboronic acid pinacol ester

CAS: 138500-85-3

4-(Bromomethyl)benzeneboronic acid pinacol ester (BBBA) is a hypochlorous acid derivative with a structural formula of C6H5BrOCH2. It is used as a fluorophore and has been shown to have anticancer activity. 4-Bromomethylbenzeneboronic acid pinacol ester reacts with hydrophobic molecules in the cell membrane, leading to disruption of the membrane and ultimately cell death. This compound can be used as an active oxygen source in biological assays, such as functional assays, because it generates reactive oxygen species and can act as a fluorescence probe for detection of biological samples.

Formula: C₁₃H₁₈BBrO₂

Purity: Min. 95 Area-%

Color and Shape: White Powder

Molecular weight: 297 g/mol

Ref: 3D-FB40268