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2,3-Diiodophenol

Base Information Edit
  • Chemical Name:2,3-Diiodophenol
  • CAS No.:408340-16-9
  • Molecular Formula:C6H4 I2 O
  • Molecular Weight:345.906
  • Hs Code.:
  • DSSTox Substance ID:DTXSID90463180
  • Nikkaji Number:J2.223.303C
  • Wikidata:Q209168
  • Mol file:408340-16-9.mol
2,3-Diiodophenol

Synonyms:2,3-diiodophenol;408340-16-9;diiodophenol;Dijodphenol;SCHEMBL605558;DTXSID90463180;MFCD08166475;MB05357;SY353146;Q209168

Suppliers and Price of 2,3-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
  • American Custom Chemicals Corporation
  • 2,3-DIIODOPHENOL 95.00%
  • 5MG
  • $ 499.82
Total 1 raw suppliers
Chemical Property of 2,3-Diiodophenol Edit
Chemical Property:
  • 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:97.1
Purity/Quality:

97% *data from raw suppliers

2,3-DIIODOPHENOL 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC(=C(C(=C1)I)I)O
Technology Process of 2,3-Diiodophenol

There total 3 articles about 2,3-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:
With sodium hydroxide; In ethanol; Heating;
DOI:10.1021/jo0508402
Guidance literature:
Multi-step reaction with 2 steps
1.1: LDA / tetrahydrofuran; hexane / 0.5 h / -78 °C
1.2: 74 percent / iodine / tetrahydrofuran; hexane / -78 - 20 °C
2.1: 82 percent / NaOH / ethanol / Heating
With sodium hydroxide; lithium diisopropyl amide; In tetrahydrofuran; ethanol; hexane;
DOI:10.1021/jo0508402
Guidance literature:
Multi-step reaction with 3 steps
1.1: NaH / tetrahydrofuran / 20 °C
1.2: 95 percent / tetrahydrofuran / 8 h / 20 °C
2.1: LDA / tetrahydrofuran; hexane / 0.5 h / -78 °C
2.2: 74 percent / iodine / tetrahydrofuran; hexane / -78 - 20 °C
3.1: 82 percent / NaOH / ethanol / Heating
With sodium hydroxide; sodium hydride; lithium diisopropyl amide; In tetrahydrofuran; ethanol; hexane;
DOI:10.1021/jo0508402
Refernces Edit
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