[A14257] CAS 98-80-6 | Benzeneboronic acid, 98+% | Alfa
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Brand: Alfa Aesar
98-80-6 | C6H7BO2 | kyselina fenylborita
Chemical Identifiers
CAS
98-80-6
Molecular Weight (g/mol)
121.93
MDL Number
MFCD00002103
Synonym
phenyl boronic acid|β-phenyl-boronic acid|phenylboronate|phenylboric acid|phenyl-boric acid|boric acid, phenyl-|usaf BO-2|acide phenylborique|kyselina fenylborita
SMILES
OB(O)C1=CC=CC=C1
InChI Key
HXITXNWTGFUOAU-UHFFFAOYSA-N
Molecular Formula
C6H7BO2
IUPAC Name
phenylboronic acid
Specifications
Appearance (Color)
White to cream
Form
Crystals or powder or crystalline powder
Assay (Aqueous acid-base Titration)
≥98.0%
Assay (HPLC)
≥98.0%
Identification (FTIR)
Conforms
설명
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.
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.
Other References:
Merck Index:14,1068Beilstein:970972
GHS Hazard and Precautionary Statements
Hazard Statements:H302
GHS H StatementH302-H315-H319-H335Harmful if swallowed.Causes skin irritation.Causes serious eye irritation.May cause respiratory irritation.
Precautionary Statements:P264-P270-P301+P312-P304+P312-P305+P351+P338-P312-P330-P501c
Risk & Safety
TSCA:YesRTECS Number:CY8575000
경고:RUO – Research Use Only
CAS98-80-6FORMULAC6H7BO2EINECS202-701-9MDLMFCD00002103
| Pakage | 10g, 250g, 50G |
|---|---|
| brand | Alfa Aesar |
