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1,2,3-Triiodobenzene

Base Information Edit
  • Chemical Name:1,2,3-Triiodobenzene
  • CAS No.:608-29-7
  • Molecular Formula:C6H3I3
  • Molecular Weight:455.803
  • Hs Code.:
  • DSSTox Substance ID:DTXSID50209642
  • Nikkaji Number:J134.630J
  • Wikidata:Q83084006
  • Mol file:608-29-7.mol
1,2,3-Triiodobenzene

Synonyms:1,2,3-TRIIODOBENZENE;Benzene, 1,2,3-triiodo-;608-29-7;TRIIODOBENZENE;SCHEMBL38083;DTXSID50209642

Suppliers and Price of 1,2,3-Triiodobenzene
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
Total 1 raw suppliers
Chemical Property of 1,2,3-Triiodobenzene Edit
Chemical Property:
  • Vapor Pressure:8.67E-05mmHg at 25°C 
  • Melting Point:116°C 
  • Refractive Index:1.8070 (estimate) 
  • Boiling Point:350.8°Cat760mmHg 
  • Flash Point:183.3°C 
  • PSA:0.00000 
  • Density:2.928g/cm3 
  • LogP:3.50040 
  • XLogP3:3.9
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:0
  • Rotatable Bond Count:0
  • Exact Mass:455.7369
  • Heavy Atom Count:9
  • Complexity:84.3
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:C1=CC(=C(C(=C1)I)I)I
Technology Process of 1,2,3-Triiodobenzene

There total 7 articles about 1,2,3-Triiodobenzene 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 N-iodo-succinimide; In 1,2-dichloro-ethane; for 24h; Photolysis; Reflux;
DOI:10.1071/CH14386
Guidance literature:
With isopentyl nitrite; In tetrahydrofuran; Yields of byproduct given. Title compound not separated from byproducts; Heating;
DOI:10.1021/jo00020a036
Guidance literature:
Multi-step reaction with 2 steps
1: palladium diacetate; iodine; [bis(acetoxy)iodo]benzene / N,N-dimethyl-formamide / 24 h / 100 °C / Sealed tube
2: N-iodo-succinimide / 1,2-dichloro-ethane / 24 h / Photolysis; Reflux
With N-iodo-succinimide; [bis(acetoxy)iodo]benzene; iodine; palladium diacetate; In 1,2-dichloro-ethane; N,N-dimethyl-formamide;
DOI:10.1071/CH14386
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