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3-Bromo-3-(4-methoxyphenyl)-3H-diazirine

Base Information
  • Chemical Name:3-Bromo-3-(4-methoxyphenyl)-3H-diazirine
  • CAS No.:95911-61-8
  • Molecular Formula:C8H7BrN2O
  • Molecular Weight:227.06
  • Hs Code.:
  • DSSTox Substance ID:DTXSID40471058
  • Nikkaji Number:J1.858.839K
  • Mol file:95911-61-8.mol
3-Bromo-3-(4-methoxyphenyl)-3H-diazirine

Synonyms:95911-61-8;3-Bromo-3-(4-methoxyphenyl)-3H-diazirine;3H-Diazirine, 3-bromo-3-(4-methoxyphenyl)-;DTXSID40471058

Suppliers and Price of 3-Bromo-3-(4-methoxyphenyl)-3H-diazirine
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
Total 3 raw suppliers
Chemical Property of 3-Bromo-3-(4-methoxyphenyl)-3H-diazirine
Chemical Property:
  • XLogP3:2.6
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:2
  • Exact Mass:225.97418
  • Heavy Atom Count:12
  • Complexity:193
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:COC1=CC=C(C=C1)C2(N=N2)Br
Technology Process of 3-Bromo-3-(4-methoxyphenyl)-3H-diazirine

There total 5 articles about 3-Bromo-3-(4-methoxyphenyl)-3H-diazirine 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 hypobromide; lithium bromide; In dimethyl sulfoxide; for 1h;
DOI:10.1021/ja00295a029
Guidance literature:
Multi-step reaction with 2 steps
1: 20 percent / 1.) sodium methoxide; 2.) NH4Cl / methanol / 25 °C / 1.) 48 h; 2.) 24 h
2: 34 percent / NaOBr, LiBr / dimethylsulfoxide / 1 h
With sodium hypobromide; sodium methylate; ammonium chloride; lithium bromide; In methanol; dimethyl sulfoxide;
DOI:10.1021/ja00295a029
Guidance literature:
Multi-step reaction with 3 steps
1: n-tetrabutylammonium azide / acetonitrile / 24 h / 25.5 °C / in the dark; var. time
2: 20 percent / 1.) sodium methoxide; 2.) NH4Cl / methanol / 25 °C / 1.) 48 h; 2.) 24 h
3: 34 percent / NaOBr, LiBr / dimethylsulfoxide / 1 h
With sodium hypobromide; sodium methylate; tetrabutylammoniun azide; ammonium chloride; lithium bromide; In methanol; dimethyl sulfoxide; acetonitrile;
DOI:10.1021/ja00295a029
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