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1,2-Dichloro-4-(4-methylbenzene-1-sulfonyl)benzene

Base Information
  • Chemical Name:1,2-Dichloro-4-(4-methylbenzene-1-sulfonyl)benzene
  • CAS No.:143538-80-1
  • Molecular Formula:C13H10Cl2O2S
  • Molecular Weight:301.193
  • Hs Code.:
  • DSSTox Substance ID:DTXSID10579797
  • Nikkaji Number:J478.597E
  • Wikidata:Q82470420
  • Mol file:143538-80-1.mol
1,2-Dichloro-4-(4-methylbenzene-1-sulfonyl)benzene

Synonyms:143538-80-1;1,2-Dichloro-4-(4-methylbenzene-1-sulfonyl)benzene;DTXSID10579797

Suppliers and Price of 1,2-Dichloro-4-(4-methylbenzene-1-sulfonyl)benzene
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of 1,2-Dichloro-4-(4-methylbenzene-1-sulfonyl)benzene
Chemical Property:
  • XLogP3:4.6
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:2
  • Exact Mass:299.9778561
  • Heavy Atom Count:18
  • Complexity:369
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC1=CC=C(C=C1)S(=O)(=O)C2=CC(=C(C=C2)Cl)Cl
Technology Process of 1,2-Dichloro-4-(4-methylbenzene-1-sulfonyl)benzene

There total 5 articles about 1,2-Dichloro-4-(4-methylbenzene-1-sulfonyl)benzene 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 eosin; In water; acetonitrile; at 20 ℃; for 12h; Irradiation; Inert atmosphere;
DOI:10.1039/c9ob00864k
Guidance literature:
With copper exchanged fluorapatite; In methanol; at 20 ℃; for 12h; Green chemistry;
DOI:10.1039/c8nj04845b
Guidance literature:
With trifluorormethanesulfonic acid; In dichloromethane; at 25 ℃; for 3h; regiospecific reaction;
DOI:10.1021/acs.joc.8b03046
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