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2-(3-chlorophenyl)acetyl chloride

Base Information
  • Chemical Name:2-(3-chlorophenyl)acetyl chloride
  • CAS No.:41904-39-6
  • Molecular Formula:C8H6Cl2O
  • Molecular Weight:189.041
  • Hs Code.:
  • Mol file:41904-39-6.mol
2-(3-chlorophenyl)acetyl chloride

Synonyms:3-chloro-benzeneacetyl chloride

Suppliers and Price of 2-(3-chlorophenyl)acetyl chloride
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • 2-(3-Chlorophenyl)acetylChloride
  • 100mg
  • $ 60.00
  • Matrix Scientific
  • (3-Chlorophenyl)acetyl chloride 95%
  • 1g
  • $ 414.00
  • CHESS?
  • CC000214:(3-Chloro-phenyl)-acetylchloride 98
  • 1 g
  • $ 120.00
  • Biosynth Carbosynth
  • (3-Chlorophenyl)acetyl chloride
  • 250 mg
  • $ 180.00
  • Biosynth Carbosynth
  • (3-Chlorophenyl)acetyl chloride
  • 100 mg
  • $ 100.00
  • Biosynth Carbosynth
  • (3-Chlorophenyl)acetyl chloride
  • 50 mg
  • $ 62.50
  • Biosynth Carbosynth
  • (3-Chlorophenyl)acetyl chloride
  • 500 mg
  • $ 300.00
  • Biosynth Carbosynth
  • (3-Chlorophenyl)acetyl chloride
  • 1 g
  • $ 450.00
  • Atlantic Research Chemicals
  • (3-Chlorophenyl)acetylchloride 95%
  • 1gm:
  • $ 187.33
  • American Custom Chemicals Corporation
  • META-CHLORO PHENYLACETIC CHLORIDE 98.00%
  • 5MG
  • $ 504.90
Total 8 raw suppliers
Chemical Property of 2-(3-chlorophenyl)acetyl chloride
Chemical Property:
Purity/Quality:

99%, *data from raw suppliers

2-(3-Chlorophenyl)acetylChloride *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Uses 2-(3-Chlorophenyl)acetyl chloride is a novel pyrrolidine MCHR1 antagonists and reduce hERG inhibition.
Technology Process of 2-(3-chlorophenyl)acetyl chloride

There total 9 articles about 2-(3-chlorophenyl)acetyl chloride which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With thionyl chloride; In dichloromethane;
DOI:10.1016/j.bmcl.2007.09.036
Guidance literature:
Multi-step reaction with 3 steps
1: potassium carbonate; tetra-(n-butyl)ammonium iodide / toluene / 5 h / 90 °C
2: sodium hydroxide; water / 100 °C
3: oxalyl dichloride; N,N-dimethyl-formamide / dichloromethane / 20 °C / Inert atmosphere
With oxalyl dichloride; water; tetra-(n-butyl)ammonium iodide; potassium carbonate; N,N-dimethyl-formamide; sodium hydroxide; In dichloromethane; toluene;
DOI:10.1021/jacs.8b13052
Guidance literature:
With oxalyl dichloride; N,N-dimethyl-formamide; In dichloromethane; at 20 ℃; Inert atmosphere;
DOI:10.1021/jacs.8b13052
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