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287512 Aldrich

3-Aminophenylboronic acid monohydrate

98%

Synonym: 3-Aminobenzeneboronic acid

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Properties

Related Categories Aryl Boronic Acids, Boronic Acids, Boronic Acids and Derivatives, Chemical Synthesis, Monosubstituted Aryl Boronic Acids,
InChI Key   XAEOVQODHLLNKX-UHFFFAOYSA-N
assay   98%
mp   93-96 °C(lit.)

Description

Packaging

1, 5 g in glass bottle

Application

Reagent used for
• Suzuki-Miyaura cross-coupling

Reagent used for Preparation of
• Gram-positive antivirulence drugs and inhibitors of Streptococcus agalactiae Stk1
• Regioisomer of Zaleplon (a sedative)
• Amphiphilic random glycopolymer, which self-assemble to form nanoparticles, with potential as a glucose-sensitive matrix
• Chemomechanical polymer that expands and contracts in blood plasma with high glucose selectivity

Price and Availability


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

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

Peer-Reviewed Papers
15

References

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