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2,6-Dichloro-α-(4-chlorophenyl)-4-nitrobenzeneacetonitrile

Base Information Edit
  • Chemical Name:2,6-Dichloro-α-(4-chlorophenyl)-4-nitrobenzeneacetonitrile
  • CAS No.:103317-59-5
  • Molecular Formula:C14H7Cl3N2O2
  • Molecular Weight:341.581
  • Hs Code.:
  • Mol file:103317-59-5.mol
2,6-Dichloro-α-(4-chlorophenyl)-4-nitrobenzeneacetonitrile

Synonyms:2-(4'-chlorophenyl)-2-(2,6-dichloro-4-nitrophenyl)acetonitrile

Suppliers and Price of 2,6-Dichloro-α-(4-chlorophenyl)-4-nitrobenzeneacetonitrile
Supply Marketing:Edit
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,?6-?Dichloro-?α-?(4-?chlorophenyl)?-?4-?nitrobenzeneacetonitrile
  • 10g
  • $ 425.00
  • Medical Isotopes, Inc.
  • 2,6-Dichloro-α-(4-chlorophenyl)-4-nitrobenzeneacetonitrile
  • 50 g
  • $ 2275.00
  • Medical Isotopes, Inc.
  • 2,6-Dichloro-α-(4-chlorophenyl)-4-nitrobenzeneacetonitrile
  • 10 g
  • $ 925.00
Total 1 raw suppliers
Chemical Property of 2,6-Dichloro-α-(4-chlorophenyl)-4-nitrobenzeneacetonitrile Edit
Chemical Property:
  • Melting Point:106 - 112oC 
  • Storage Temp.:Refrigerator 
  • Solubility.:Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly) 
Purity/Quality:

2,?6-?Dichloro-?α-?(4-?chlorophenyl)?-?4-?nitrobenzeneacetonitrile *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Uses 2,6-Dichloro-α-(4-chlorophenyl)-4-nitrobenzeneacetonitrile is used in the synthesis of anticoccidial triazine compounds.
Technology Process of 2,6-Dichloro-α-(4-chlorophenyl)-4-nitrobenzeneacetonitrile

There total 3 articles about 2,6-Dichloro-α-(4-chlorophenyl)-4-nitrobenzeneacetonitrile 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:
3,4,5-trichloronitrobenzen; With tetrabutylammomium bromide; sodium hydroxide; In water; for 0.5h;
p-chlorobenzyl cyanide; In tetrahydrofuran; water; at 60 ℃; for 8h;
Guidance literature:
Multi-step reaction with 2 steps
1.1: sulfuric acid; sodium nitrite / 0.33 h / 5 - 70 °C
1.2: 0.5 h
1.3: 1 h / 25 - 70 °C
2.1: sodium hydroxide / butanone / 2 h / 50 °C
With sulfuric acid; sodium hydroxide; sodium nitrite; In butanone;
Refernces Edit
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