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2-Benzyloxy-4-iodophenol

Base Information
  • Chemical Name:2-Benzyloxy-4-iodophenol
  • CAS No.:289471-92-7
  • Molecular Formula:C13H11IO2
  • Molecular Weight:326.134
  • Hs Code.:
  • DSSTox Substance ID:DTXSID00573002
  • Wikidata:Q82461554
  • Mol file:289471-92-7.mol
2-Benzyloxy-4-iodophenol

Synonyms:2-Benzyloxy-4-iodophenol;289471-92-7;2-(Benzyloxy)-4-iodophenol;4-iodo-2-phenylmethoxyphenol;4-Iodo-2-(phenylmethoxy)phenol;SCHEMBL17685895;DTXSID00573002;SUUAJTJMEHPEDV-UHFFFAOYSA-N;CS-0527518;G63100;A846303

Suppliers and Price of 2-Benzyloxy-4-iodophenol
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
  • TRC
  • 2-Benzyloxy-4-iodophenol
  • 5g
  • $ 1540.00
  • TRC
  • 2-Benzyloxy-4-iodophenol
  • 500mg
  • $ 195.00
  • Crysdot
  • 2-Benzyloxy-4-iodophenol 95+%
  • 5g
  • $ 2300.00
Total 2 raw suppliers
Chemical Property of 2-Benzyloxy-4-iodophenol
Chemical Property:
  • PSA:29.46000 
  • LogP:3.57580 
  • XLogP3:3.7
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:3
  • Exact Mass:325.98038
  • Heavy Atom Count:16
  • Complexity:204
Purity/Quality:

97% *data from raw suppliers

2-Benzyloxy-4-iodophenol *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:C1=CC=C(C=C1)COC2=C(C=CC(=C2)I)O
  • Uses 2-Benzyloxy-4-iodophenol is used in the preparation of isotope labelled Quercetin (Q509500) conjugates.
Technology Process of 2-Benzyloxy-4-iodophenol

There total 3 articles about 2-Benzyloxy-4-iodophenol 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 hypochlorite; sodium iodide; sodium hydroxide; In methanol; at -10 - 10 ℃; for 0.166667h;
Guidance literature:
Multi-step reaction with 2 steps
1.1: NaOH / methanol / 0 - 3 °C
1.2: 32 percent / methanol / 2 h / Heating
2.1: NaI; NaOH / methanol
2.2: 35 percent / aq. NaClO / 1 h / 0 - 2 °C
With sodium hydroxide; sodium iodide; In methanol;
DOI:10.1021/ja0535357
Guidance literature:
Multi-step reaction with 2 steps
1.1: NaOH / methanol / 0 - 3 °C
1.2: 32 percent / methanol / 2 h / Heating
2.1: NaI; NaOH / methanol
2.2: 35 percent / aq. NaClO / 1 h / 0 - 2 °C
With sodium hydroxide; sodium iodide; In methanol;
DOI:10.1021/ja0535357
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