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471917 Aldrich

3,4-Dichlorophenylboronic acid

Synonym: 3,4-Dichlorobenzeneboronic acid

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Properties

Related Categories Aryl Boronic Acids, Boronic Acids, Boronic Acids and Derivatives, Chemical Synthesis, Disubstituted Aryl Boronic Acids,
InChI Key   JKIGHOARKAIPJI-UHFFFAOYSA-N
mp   280-285 °C(lit.)

Description

Packaging

5, 25 g in glass bottle

Application

Reactant involved in:
• Lithiation/borylation-protodeboronation of homoallyl carbamates
• Suzuki coupling reactions

Precursor / reactant involved in synthesis of biologically active molecules including:
• Mycobacterium tuberculosis H37Rv chorismate mutase inhibitors
• Pyrrole derivatives as PDE4B inhibitors
• Nitrovinyl biphenyls as anticancer agents
• Dual immunosuppressive and anti-inflammatory agents
• Pyrazolopyrimidines as Cryptosporidium and Toxoplasma CDPK1 inhibitors

Price and Availability


KitAlysis - Increasing Catalysis Productivity
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

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