3-Chlorophenylboronic acid
3-Chlorophenylboronic acid
  • CAS No.:63503-60-6
Other grades of this product :
3-Chlorophenylboronic acid Basic information
Product Name:3-Chlorophenylboronic acid
Synonyms:B-(3-chlorophenyl)-boronic acid;3-Chlorobenzeneboronic acid 98%;3-Chlorophenylboronic;3-Chlorophenylboornic acid;RARECHEM AH PB 0179;3-CHLOROPHENYLBORNIC ACID;3-CHLOROPHENYLBORONIC ACID;3-CHLOROBENZENEBORONIC ACID
CAS:63503-60-6
MF:C6H6BClO2
MW:156.37
EINECS:628-786-6
Product Categories:Boronate Ester;Potassium Trifluoroborate;Boronic acids;Aryl;Halogenated;Organoborons;blocks;BoronicAcids;Boronic Acid series;Substituted Boronic Acids;Boronic Acid;B (Classes of Boron Compounds);Boronic Acids;Boronic Acids and Derivatives
Mol File:63503-60-6.mol
3-Chlorophenylboronic acid Chemical Properties
Melting point 185-189 °C(lit.)
Boiling point 311.4±44.0 °C(Predicted)
density 1.32±0.1 g/cm3(Predicted)
storage temp. Inert atmosphere,Room Temperature
solubility soluble in Methanol
pka7.55±0.10(Predicted)
form Crystalline Powder or Needles
color White to light yellow-green
Water Solubility Slightly soluble in water. soluble in ether, tetrahydrofuran,, dimethyl sulfoxide, dimethyl formamide, methanol.
BRN 2936343
InChIKeySDEAGACSNFSZCU-UHFFFAOYSA-N
CAS DataBase Reference63503-60-6(CAS DataBase Reference)
Safety Information
Hazard Codes Xn,Xi
Risk Statements 20/21/22-36/37/38
Safety Statements 36-37/39-26
WGK Germany 3
HazardClass IRRITANT
HS Code 29163990
MSDS Information
ProviderLanguage
SigmaAldrich English
ACROS English
ALFA English
3-Chlorophenylboronic acid Usage And Synthesis
Chemical Propertieswhite to light yellow-green crystalline powder or
Usessuzuki reaction
UsesIt is employed as a reactant involved in 1,4-conjugate addition reactions with ethenesulfonamides to form arylethanesulfonamides, Suzuki-Miyaura reactions with dibromotrifluoromethylbenzene, cross-coupling reactions with diazoesters3 or potassium cyanate. It is involved in the synthesis of biarylketones and phthalides and synthesis of inhibitors including PDE4 inhibitors6 among others.
UsesReactant involved in:
  • 1,4-conjugate addition reactions with ethenesulfonamides to form arylethanesulfonamides
  • Suzuki-Miyaura reactions with dibromotrifluoromethylbenzene
  • Cross-coupling reactions with diazoesters or potassium cyanate
  • Synthesis of biarylketones and phthalides
  • Synthesis of inhibitors including PDE4 inhibitors among others
3-Chlorophenylboronic acid Preparation Products And Raw materials
Preparation Products3-CHLOROPHENYLBORONIC ACID, PINACOL ESTER

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