2,6-Dichlorobenzoyl chloride

2,6-Dichlorobenzoyl chloride Basic information
Product Name:2,6-Dichlorobenzoyl chloride
Synonyms:Benzoyl chloride, 2,6-dichloro-;DICHLOROBENZOYLCHLORIDE(2,6-);2,6-DICHLOROBENZOYL CHLORIDE;2,6-DICHLORBENZOYL CHLORIDE;2,6-DICHLOROBENZOYL CHLORIDE 98+%;Benzoyl chloride, 2,6-dichloro- (6CI,7CI,8CI,9CI);2,6-Dichlorobenzoyl;2,6-Dichlorobenzoic acid chloride
CAS:4659-45-4
MF:C7H3Cl3O
MW:209.46
EINECS:225-102-4
Product Categories:Acid Halides;Carbonyl Compounds;ACIDHALIDE;Organic Building Blocks
Mol File:4659-45-4.mol
2,6-Dichlorobenzoyl chloride Structure
2,6-Dichlorobenzoyl chloride Chemical Properties
Melting point 15-17 °C
Boiling point 142-143 °C/21 mmHg (lit.)
density 1.462 g/mL at 25 °C (lit.)
refractive index n20/D 1.560(lit.)
Fp >230 °F
storage temp. Inert atmosphere,2-8°C
form Liquid
color Clear colorless to light yellow or light pink
Water Solubility Miscible with alcohol, ether and acetone. Slightly miscible with heptane. Immiscible with water.
Sensitive Moisture Sensitive
BRN 639531
CAS DataBase Reference4659-45-4(CAS DataBase Reference)
NIST Chemistry Reference2,6-Dichlorobenzoyl chloride(4659-45-4)
Safety Information
Hazard Codes C
Risk Statements 34
Safety Statements 26-27-36/37/39-45
RIDADR UN 3265 8/PG 2
WGK Germany 1
10-19-21
HazardClass 8
PackingGroup II
HS Code 29163900
MSDS Information
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2,6-Dichlorobenzoyl chloride Usage And Synthesis
Chemical PropertiesClear slightly yellow liquid
Uses2,6-Dichlorobenzoyl chloride acts as an important intermediate in organic synthesis, pharmaceuticals, agrochemicals and dyestuffs. It is employed in the substrate activity screening method for the rapid development of novel substrates and their conversion into non-peptidic inhibitors of Cys and Ser proteases. It is also used in the preparation of 1-acyliridoles and (-)-aspicilin. In addition to this, it undergoes esterification of (fluoren-9-ylmethoxy)carbonyl (Fmoc)-amino acids to 4-alkoxybenzyl alcohol polystyrene.
Uses2,6-Dichlorobenzoyl chloride was used:
  • in substrate activity screening method for the rapid development of novel substrates and their conversion into non-peptidic inhibitors of Cys and Ser proteases
  • in the synthesis of 1-acyliridoles
  • in enantiocontrolled total synthesis of (-)-aspicilin
General Description2,6-Dichlorobenzoyl chloride participates in esterification of (fluoren-9-ylmethoxy)carbonyl (Fmoc)-amino acids to 4-alkoxybenzyl alcohol polystyrene.
Purification MethodsReflux the acid chloride for 2hours with excess of acetyl chloride (3 volumes), distil off AcCl followed by the benzoyl chloride. Store it away from moisture. It is an IRRITANT.[Beilstein 9 III 1377.]
Methylene Chloride Benzoyl peroxide 4-Nitrobenzoyl chloride Calcium chloride Sodium chloride 2,4,6-Trichlorobenzoyl chloride 4-tert-Butylbenzoyl chloride Ferric chloride 2',4'-Dichloroacetophenone 3,5-DICHLOROBENZOYL CHLORIDE 96+%,3,5-DICHLOROBENZOYL CHLORIDE 98+%,3,5-DICHLOROBENZOYL CHLORIDE 4-Chlorobenzoyl chloride Benzoyl chloride Potassium chloride 2,3-DICHLOROBENZOYL CHLORIDE 2-​[[(2-​ethylphenyl)​(2-​hydroxyethyl)​amino]​methyl]​-​3,​3-​difluoro-Propanenitrile p-Toluoyl chloride 2-Chlorobenzoyl chloride 4-Dichlorobenzoyl Chloride 99%,2,4-Dichlorobenzoyl chloride

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