Basic information Safety Supplier Related
ChemicalBook >  Product Catalog >  Inorganic chemistry >  Inorganic salts >  Borides, borates and borate >  (3-CHLORO-4-METHOXYCARBONYL)BENZENEBORONIC ACID

(3-CHLORO-4-METHOXYCARBONYL)BENZENEBORONIC ACID

Basic information Safety Supplier Related

(3-CHLORO-4-METHOXYCARBONYL)BENZENEBORONIC ACID Basic information

Product Name:
(3-CHLORO-4-METHOXYCARBONYL)BENZENEBORONIC ACID
Synonyms:
  • (4-(Methoxycarbonyl)-3-chlorophenyl)boronic acid
  • 3-Chloro-4-(methoxycarbonyl)phenylboronic Acid (contains varying amounts of Anhydride)
  • AKOS BRN-0545
  • (3-CHLORO-4-METHOXYCARBONYL)BENZENEBORONIC ACID
  • 3-CHLORO-4-(METHOXYCARBONYL)PHENYLBORONIC ACID
  • METHYL 4-BORONO-2-CHLOROBENZOATE
  • 3-Chloro-4-(methoxycarbonyl)benzeneboronic acid 97%
  • (3-Chloro-4-(methoxycarbonyl)phenyl)boronic acid, 99.8%
CAS:
603122-82-3
MF:
C8H8BClO4
MW:
214.41
EINECS:
600-419-4
Product Categories:
  • blocks
  • BoronicAcids
  • Carboxes
Mol File:
603122-82-3.mol
More
Less

(3-CHLORO-4-METHOXYCARBONYL)BENZENEBORONIC ACID Chemical Properties

Melting point:
174-178
storage temp. 
Inert atmosphere,2-8°C
solubility 
soluble in Methanol
form 
powder to crystal
color 
White to Almost white
More
Less

Safety Information

Hazard Codes 
Xi
Hazard Note 
Irritant
HS Code 
2931900090
More
Less

(3-CHLORO-4-METHOXYCARBONYL)BENZENEBORONIC ACID Usage And Synthesis

Uses

3-Chloro-4-methoxycarbonylphenylboronic acid

Synthesis

To a solution of methyl 2-chloro-4-bromobenzoate (31.4 mmol) in dioxane (154 mL) was added pinacol ester of bis(boronic acid) (8.6 g, 31.4 mmol), PdCl2(PPh3)2 (0.42 mmol), and KOAc (94.2 mmol), and the mixture was stirred for 2-6 hr at 100 ??C under nitrogen. The mixture was diluted with EtOAc and water. The organic layer was separated, washed with brine, dried over MgSO4 and evaporated. The residue was purified by silica gel column chromatography (hexane/EtOAc 5/1) to give 3-chloro-4-methoxycarbonylphenylboronic acid pinacol ester. To a suspension of the above product (29.4 mmol) in acetone (175 mL) and water (175 mL) was added NH4OAc (66.2 mmol) and NaIO4 (14.2 g, 66.4 mmol) and the mixture was stirred for 15 hours at room temperature. The solvent was evaporated and the residue was diluted with EtOAc. The organic layer was separated, washed with water and brine, dried over MgSO4 and evaporated under reduced pressure to give the title compound as a white solid.

(3-CHLORO-4-METHOXYCARBONYL)BENZENEBORONIC ACIDSupplier

J & K SCIENTIFIC LTD.
Tel
18210857532; 18210857532
Email
jkinfo@jkchemical.com
Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
4006356688 18621169109
Email
market03@meryer.com
Alfa Aesar
Tel
400-6106006
Email
saleschina@alfa-asia.com
BeiJing Hwrk Chemicals Limted
Tel
0757-86329057 18934348241
Email
sales4.gd@hwrkchemical.com
Energy Chemical
Tel
021-021-58432009 400-005-6266
Email
sales8178@energy-chemical.com