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1,2-Diiodo-4,5-dinitrobenzene

Base Information
  • Chemical Name:1,2-Diiodo-4,5-dinitrobenzene
  • CAS No.:29270-47-1
  • Molecular Formula:C6H2 I2 N2 O4
  • Molecular Weight:419.902
  • Hs Code.:2904909090
  • DSSTox Substance ID:DTXSID10454090
  • Nikkaji Number:J1.192.717C
  • Wikidata:Q82275425
  • Mol file:29270-47-1.mol
1,2-Diiodo-4,5-dinitrobenzene

Synonyms:1,2-diiodo-4,5-dinitrobenzene;1,2-diiodo-4,5-dinitro-benzene;29270-47-1;Benzene, 1,2-diiodo-4,5-dinitro-;SCHEMBL243414;1,2-dinitro-4,5-diiodobenzene;DTXSID10454090;KAQQACPCRNDISO-UHFFFAOYSA-N;1,2-dinitro-4,5-di-iodobenzene;AKOS015964735

Suppliers and Price of 1,2-Diiodo-4,5-dinitrobenzene
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
  • American Custom Chemicals Corporation
  • 1,2-DIIODO-4,5-DINITRO-BENZENE 95.00%
  • 10MG
  • $ 1732.50
  • American Custom Chemicals Corporation
  • 1,2-DIIODO-4,5-DINITRO-BENZENE 95.00%
  • 1MG
  • $ 721.88
Total 1 raw suppliers
Chemical Property of 1,2-Diiodo-4,5-dinitrobenzene
Chemical Property:
  • PSA:91.64000 
  • LogP:3.75860 
  • XLogP3:2.9
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:0
  • Exact Mass:419.81040
  • Heavy Atom Count:14
  • Complexity:225
Purity/Quality:

1,2-DIIODO-4,5-DINITRO-BENZENE 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=C(C(=CC(=C1I)I)[N+](=O)[O-])[N+](=O)[O-]
Technology Process of 1,2-Diiodo-4,5-dinitrobenzene

There total 2 articles about 1,2-Diiodo-4,5-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 sulfuric acid; sulfur trioxide; iodine; at 120 ℃; for 1.33333h;
DOI:10.3390/molecules26113163
Guidance literature:
Guidance literature:
With ammonia; In tetrahydrofuran; at 20 ℃; for 10h;
DOI:10.1021/jo050926v
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