missing translation for 'onlineSavingsMsg'
Learn More

Benzeneboronic acid, 98+%, Thermo Scientific Chemicals

Catalog Number p-7021781
Click to view available options
Quantity:
10 g
50 g
250 g
98-80-6
C6H7BO2
121.93
MFCD00002103
HXITXNWTGFUOAU-UHFFFAOYSA-N
benzeneboronic acid, boronic acid, phenyl, phenyl boronic acid, phenylboric acid, dihydroxyphenylborane, phenyldihydroxyborane, dihydroxy phenyl borane, phenylboronicacid, borophenylic acid, usaf bo-2
66827
CHEBI:44923
phenylboronic acid
OB(O)C1=CC=CC=C1
98-80-6
C6H7BO2
121.93
MFCD00002103
HXITXNWTGFUOAU-UHFFFAOYSA-N
benzeneboronic acid, boronic acid, phenyl, phenyl boronic acid, phenylboric acid, dihydroxyphenylborane, phenyldihydroxyborane, dihydroxy phenyl borane, phenylboronicacid, borophenylic acid, usaf bo-2
66827
CHEBI:44923
phenylboronic acid
OB(O)C1=CC=CC=C1

Benzeneboronic acid is widely utilized in various cross coupling reactions for example Mizoroki-Heck and Suzuki-Miyaura coupling reactions, etc. It serves as a receptor for carbohydrates, antimicrobial agents and enzyme inhibitors in biological reactions. It acts as a reagent in palladium-catalyzed stereoselective Heck-type reaction and as a catalyst in Ni(II) pincer complex and Pd(II) pyridoxal hydrazone metallacycles. It is also employed as a sensor for neutron capture therapy for cancer, transmembrane transport and bioconjugation and labeling of proteins and cell surface.

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 Scientific Chemicals.

Applications
Benzeneboronic acid is widely utilized in various cross coupling reactions for example Mizoroki-Heck and Suzuki-Miyaura coupling reactions, etc. It serves as a receptor for carbohydrates, antimicrobial agents and enzyme inhibitors in biological reactions. It acts as a reagent in palladium-catalyzed stereoselective Heck-type reaction and as a catalyst in Ni(II) pincer complex and Pd(II) pyridoxal hydrazone metallacycles. It is also employed as a sensor for neutron capture therapy for cancer, transmembrane transport and bioconjugation and labeling of proteins and cell surface.

Solubility
Slightly soluble in water.

Notes
Hygroscopic. Keep container tightly closed in a dry and well-ventilated place. Incompatible with strong oxidizing agents. Avoid moisture exposure.
TRUSTED_SUSTAINABILITY
Melting Point 214°C to 219°C
Quantity 10 g
Beilstein 970972
Sensitivity Hygroscopic
Merck Index 14,1068
Solubility Information Slightly soluble in water.
Formula Weight 121.93
Percent Purity ≥98%
Chemical Name or Material Benzeneboronic acid

RUO – Research Use Only

missing translation for 'provideContentCorrection'

missing translation for 'productTitle'