• USA Home
  • 471933 - 4-Iodophenylboronic acid

EMAIL THIS PAGE TO A FRIEND
471933 Sigma-Aldrich

4-Iodophenylboronic acid

≥95.0%

Synonym: B-(4-iodophenyl)-boronic acid, p-iodo-benzeneboronic acid, p-Iodophenylboronic acid

Purchase

Properties

Related Categories Aryl Boronic Acids, Boronic Acids, Boronic Acids and Derivatives, Chemical Synthesis, Monosubstituted Aryl Boronic Acids,
InChI Key   PELJYVULHLKXFF-UHFFFAOYSA-N
assay   ≥95.0%
mp   326-330 °C (lit.)

Description

Application

Reagent used for
• Copper-mediated ligandless aerobic fluoroalkylation
• Palladium-catalyzed aerobic oxidative cross-coupling reactions
• Recyclable magnetic-nanoparticle-supported palladium catalyst for the Suzuki coupling reactions
• Oxidative hydroxylation using a copper (Cu) catalyst
• Ligand-free palladium-catalyzed Suzuki-Miyaura cross-coupling
• Homocoupling using gold salts as a catalyst
• Ruthenium (Ru)-catalyzed cross-coupling
• CuI-catalyzed Suzuki coupling reactions
• Palladium-catalyzed domino Heck-Mizoroki/Suzuki-Miyaura reactions
• Manganese triacetate-mediated radical additions of arylboronic acids to alkenes

Reagent used in Preparation of
• Pleuromutilin derivatives for ribosomal binding and antibacterial activity via "Click Chemistry"
• Liquid crystalline polyacetylene derivatives

Packaging

5, 25 g in glass bottle

Other Notes

Contains varying amounts of anhydride

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

Documents

Certificate of Analysis (COA)

Please Enter a Lot Number

Certificate of Origin (COO)

Please Enter a Lot Number
Protocols & Articles

Articles

Arylboronic Acids

We are 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 a cy...
ChemFiles 2001, 1.1, 5.
Keywords: Building blocks, Coupling reactions, Dehydration reaction, Suzuki coupling

Boronic Acids - ChemFiles 2007

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...
ChemFiles 2007, 7.7, 3.
Keywords: Coupling reactions, Dehydration reaction, Suzuki coupling

Peer-Reviewed Papers
15

References

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?