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2-Bromo-3-(2-bromoethyl)-6-methoxyphenol

Base Information Edit
  • Chemical Name:2-Bromo-3-(2-bromoethyl)-6-methoxyphenol
  • CAS No.:105728-94-7
  • Molecular Formula:C9H10Br2O2
  • Molecular Weight:309.985
  • Hs Code.:2909500000
  • DSSTox Substance ID:DTXSID80575185
  • Wikidata:Q82464473
  • Mol file:105728-94-7.mol
2-Bromo-3-(2-bromoethyl)-6-methoxyphenol

Synonyms:2-Bromo-3-(2-bromoethyl)-6-methoxyphenol;105728-94-7;DTXSID80575185

Suppliers and Price of 2-Bromo-3-(2-bromoethyl)-6-methoxyphenol
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 2-Bromo-3-(2-bromoethyl)-6-methoxyphenol Edit
Chemical Property:
  • PSA:29.46000 
  • LogP:3.10070 
  • XLogP3:3.2
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:3
  • Exact Mass:309.90271
  • Heavy Atom Count:13
  • Complexity:155
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:COC1=C(C(=C(C=C1)CCBr)Br)O
Technology Process of 2-Bromo-3-(2-bromoethyl)-6-methoxyphenol

There total 7 articles about 2-Bromo-3-(2-bromoethyl)-6-methoxyphenol 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 carbon tetrabromide; triphenylphosphine; In acetonitrile; at 25 ℃; for 1h;
DOI:10.1021/jo00379a038
Guidance literature:
Multi-step reaction with 6 steps
1: 70 percent / Br2, NaOAc, HOAc / 2 h / 25 °C
2: 80 percent / NaH / dimethylformamide / 18 h / 25 °C
3: 86 percent / 5 N NaOH / benzene / 12 h / 25 °C
4: 1.) (Sia)2BH, 2.) H2O2, NaOH / 1.) THF, 0 deg C, 1 h, 2.) THF, 0 deg C, 1 h
5: 93 percent / TsOH / methanol / 4 h / 25 °C
6: 92 percent / CBr4, (C6H5)3P / acetonitrile / 1 h / 25 °C
With sodium hydroxide; carbon tetrabromide; (Sia)2BH; dihydrogen peroxide; bromine; sodium acetate; sodium hydride; toluene-4-sulfonic acid; acetic acid; triphenylphosphine; In methanol; N,N-dimethyl-formamide; acetonitrile; benzene;
DOI:10.1021/jo00379a038
Guidance literature:
Multi-step reaction with 5 steps
1: 80 percent / NaH / dimethylformamide / 18 h / 25 °C
2: 86 percent / 5 N NaOH / benzene / 12 h / 25 °C
3: 1.) (Sia)2BH, 2.) H2O2, NaOH / 1.) THF, 0 deg C, 1 h, 2.) THF, 0 deg C, 1 h
4: 93 percent / TsOH / methanol / 4 h / 25 °C
5: 92 percent / CBr4, (C6H5)3P / acetonitrile / 1 h / 25 °C
With sodium hydroxide; carbon tetrabromide; (Sia)2BH; dihydrogen peroxide; sodium hydride; toluene-4-sulfonic acid; triphenylphosphine; In methanol; N,N-dimethyl-formamide; acetonitrile; benzene;
DOI:10.1021/jo00379a038
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