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2-(2-chloroethyl)-1,3-dinitrobenzene

Base Information Edit
  • Chemical Name:2-(2-chloroethyl)-1,3-dinitrobenzene
  • CAS No.:52536-99-9
  • Molecular Formula:C8H7ClN2O4
  • Molecular Weight:230.608
  • Hs Code.:
  • Mol file:52536-99-9.mol
2-(2-chloroethyl)-1,3-dinitrobenzene

Synonyms:2-(2-chloroethyl)-1,3-dinitrobenzene

Suppliers and Price of 2-(2-chloroethyl)-1,3-dinitrobenzene
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
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  • price
Total 1 raw suppliers
Chemical Property of 2-(2-chloroethyl)-1,3-dinitrobenzene Edit
Chemical Property:
  • PSA:91.64000 
  • LogP:3.33070 
Purity/Quality:

99%,98% *data from raw suppliers

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

SDS file from LookChem

Useful:
Technology Process of 2-(2-chloroethyl)-1,3-dinitrobenzene

There total 2 articles about 2-(2-chloroethyl)-1,3-dinitrobenzene 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 pyridine; r.t., 1h then 80 degC, 15min.;
DOI:10.1002/jhet.5570250202
Guidance literature:
Multi-step reaction with 2 steps
1: 77 percent / potassium t-butoxide / dimethylsulfoxide; 2-methyl-propan-2-ol / r.t., 5min. then 70-75 degC, 10min.
2: 74 percent / SOCl2 / pyridine / r.t., 1h then 80 degC, 15min.
With thionyl chloride; potassium tert-butylate; In pyridine; dimethyl sulfoxide; tert-butyl alcohol;
DOI:10.1002/jhet.5570250202
Guidance literature:
With hydrogenchloride; iron; In ethanol; for 2h; Heating;
DOI:10.1002/jhet.5570250202
Refernces Edit
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