• USA Home
  • A71751 - 3-Aminophenylboronic acid hemisulfate salt

EMAIL THIS PAGE TO A FRIEND
A71751 Aldrich

3-Aminophenylboronic acid hemisulfate salt

≥95%

Synonym: (3-aminophenyl)-boronic acid sulfate (2:1), (3-Aminophenyl)boric acid hemisulfate, (m-Aminophenyl)boronic acid hemisulfate, 3-Aminobenzeneboronic acid hemisulfate salt, Bis[3-dihydroxyboranyl)benzenaminium] sulfate

Purchase

Properties

Related Categories Aryl Boronic Acids, Boronic Acids, Boronic Acids and Derivatives, Chemical Synthesis, Monosubstituted Aryl Boronic Acids,
InChI Key   UKTAURVTSWDIQR-UHFFFAOYSA-N
assay   ≥95%
mp   ≥300 °C

Description

Packaging

25 g in poly bottle

5 g in glass bottle

Price and Availability


KitAlysis - Increasing Catalysis Productivity

Cross-Coupling Guide
Safety & Documentation

Safety Information

Symbol 
GHS07  GHS07
Signal word 
Warning
Hazard statements 
Precautionary statements 
Personal Protective Equipment 
RIDADR 
NONH for all modes of transport
WGK Germany 
3
Protocols & Articles

Articles

Arylboronic Acids

Aldrich is pleased to present its complete selection of arylboronic acids, the building blocks of the Suzuki coupling experiment. Most arylboronic acids readily undergo dehydration reactions to give ...
Aldrich ChemFiles 2001, 1.1, 5.
Keywords: Building blocks, Coupling reactions, Dehydration reaction, Suzuki coupling

Boronic Acids - Aldrich ChemFiles 2007, 7.7, 3.

Most boronic acids readily undergo dehydration reactions to give a cyclic (trimer) anhydride. Our selection of boronic acids may contain varying amounts of this cyclic anhydride. Fortunately, the aci...
Aldrich ChemFiles 2007, 7.7, 3.
Keywords: Chemfiles, Coupling reactions, Dehydration reaction, Suzuki coupling

Related Products

Technical Service:

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Bulk Ordering & Pricing:

Need larger quantities for your development, manufacturing or research applications?