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3,5-Diiodophenol

Base Information Edit
  • Chemical Name:3,5-Diiodophenol
  • CAS No.:20981-79-7
  • Molecular Formula:C6H4I2O
  • Molecular Weight:345.906
  • Hs Code.:2908199090
  • DSSTox Substance ID:DTXSID80573449
  • Nikkaji Number:J801.820K
  • Wikidata:Q223017
  • Mol file:20981-79-7.mol
3,5-Diiodophenol

Synonyms:3,5-DIIODOPHENOL;20981-79-7;Phenol, 3,5-diiodo-;SCHEMBL1687060;DTXSID80573449;MFCD12405421;MB11867;SY162515;CS-0237106;EN300-178001;Q223017

Suppliers and Price of 3,5-Diiodophenol
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
  • Matrix Scientific
  • 3,5-Diiodophenol 95+%
  • 250mg
  • $ 265.00
  • Matrix Scientific
  • 3,5-Diiodophenol 95+%
  • 1g
  • $ 588.00
  • American Custom Chemicals Corporation
  • 3,5-DIIODOPHENOL 95.00%
  • 5MG
  • $ 500.18
  • AK Scientific
  • 3,5-Diiodophenol
  • 1g
  • $ 843.00
Total 8 raw suppliers
Chemical Property of 3,5-Diiodophenol Edit
Chemical Property:
  • PKA:pK1:8.103 (25°C) 
  • PSA:20.23000 
  • LogP:2.60140 
  • XLogP3:2.9
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:0
  • Exact Mass:345.83516
  • Heavy Atom Count:9
  • Complexity:87.1
Purity/Quality:

99%min *data from raw suppliers

3,5-Diiodophenol 95+% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=C(C=C(C=C1I)I)O
Technology Process of 3,5-Diiodophenol

There total 7 articles about 3,5-Diiodophenol 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:
1,3,5-Triiodobenzene; With n-butyllithium; In diethyl ether; hexane; at -78 - 25 ℃;
With sodium hydroxide; dihydrogen peroxide; for 3h;
DOI:10.1021/jo035311h
Guidance literature:
3,5-diiodoaniline; With sulfuric acid; at 0 ℃; for 0.5h; Inert atmosphere; Schlenk technique;
With sodium nitrite; at 0 ℃; for 2h; Inert atmosphere; Schlenk technique;
With sulfuric acid; for 0.5h; Inert atmosphere; Schlenk technique;
DOI:10.1002/chem.201504598
Guidance literature:
Multi-step reaction with 2 steps
1.1: sodium dithionit / H2O; 2-methoxy-ethanol / 3 h / Heating
1.2: 94 percent / conc. HCl / H2O; 2-methoxy-ethanol / 1 h / Heating
With sodium dithionite; In 2-methoxy-ethanol; water;
DOI:10.1021/ja003990x
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