ChemicalBook Product Catalog Chemical Reagents Organic reagents Boric acid 4-Iodophenylboronic acid

4-Iodophenylboronic acid

4-Iodophenylboronic acid Basic information
Product Name:4-Iodophenylboronic acid
Synonyms:4-IODOBENZENEBORONIC ACID;4-IODOPHENYLBORONIC ACID;RARECHEM AH PB 0035;P-IODOPHENYLBORONIC ACID;4-Iodophenylboronic acid,97%;p-Iodophenylboromc Acid;4-Iodophenylboronic acid ,98%;4-Iodophenylboronic
CAS:5122-99-6
MF:C6H6BIO2
MW:247.83
EINECS:
Product Categories:Boronic acid;Aryl;Boronic Acids;Boronic Acids and Derivatives;Boronic Acids
Mol File:5122-99-6.mol
4-Iodophenylboronic acid Structure
4-Iodophenylboronic acid Chemical Properties
Melting point 326-330 °C (lit.)
Boiling point 333.1±44.0 °C(Predicted)
density 1.95±0.1 g/cm3(Predicted)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility soluble in Methanol
pka8.29±0.10(Predicted)
form Powder
color Light beige
Water Solubility 25 g/L
Sensitive Light Sensitive
InChIKeyPELJYVULHLKXFF-UHFFFAOYSA-N
CAS DataBase Reference5122-99-6(CAS DataBase Reference)
Safety Information
Hazard Codes Xn,Xi
Risk Statements 22-36/37/38
Safety Statements 26-36-37/39
WGK Germany 3
HazardClass IRRITANT
HS Code 29319090
MSDS Information
ProviderLanguage
ACROS English
SigmaAldrich English
4-Iodophenylboronic acid Usage And Synthesis
Chemical PropertiesWhite crystalline powder
UsesReagent 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
Usessuzuki reaction
4-Iodophenylboronic acid Preparation Products And Raw materials
Preparation Products4-Iodobiphenyl-->4,4'-Diiodobiphenyl-->6-Iodoquinoline-->4'-iodo-2-nitro-1,1'-biphenyl
2-Iodophenylboronic Acid Pinacol Ester 3-IODOPHENYLBORONIC ACID 2-FLUORO-4-IODO PHENYL BORONIC ACID 2-Iodophenylboronic acid (Diacetoxyiodo)benzene 2-FLUORO-4-IODOPHENYLBORONIC ACID Zinc borate Phenylboronic acid 4-Iodophenylboronic acid MIDA ester 2-FLUORO-6-IODOPHENYLBORONIC ACID 4-Iodoanisole 6-BROMO-2-FLUORO-3-IODOPHENYLBORONIC ACID 3-Iodophenylboronic acid pinacol ester 2-FLUORO-3-IODOPHENYLBORONIC ACID 2-IODOPHENYLBORONIC ACID 4-Iodophenylboronic acid pinacol ester 3-Iodophenylboronic acid MIDA ester 2-FLUORO-5-IODOPHENYLBORONIC ACID
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