Welcome to LookChem.com Sign In|Join Free
  • or

Encyclopedia

Oxirane, 2-[difluoro(methylthio)methyl]-2-phenyl-

Base Information Edit
  • Chemical Name:Oxirane, 2-[difluoro(methylthio)methyl]-2-phenyl-
  • CAS No.:192862-21-8
  • Molecular Formula:C10H10F2OS
  • Molecular Weight:216.252
  • Hs Code.:
  • DSSTox Substance ID:DTXSID30441422
  • Mol file:192862-21-8.mol
Oxirane, 2-[difluoro(methylthio)methyl]-2-phenyl-

Synonyms:Oxirane, 2-[difluoro(methylthio)methyl]-2-phenyl-;192862-21-8;DTXSID30441422

Suppliers and Price of Oxirane, 2-[difluoro(methylthio)methyl]-2-phenyl-
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 0 raw suppliers
Chemical Property of Oxirane, 2-[difluoro(methylthio)methyl]-2-phenyl- Edit
Chemical Property:
  • XLogP3:2.6
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:3
  • Exact Mass:216.04204244
  • Heavy Atom Count:14
  • Complexity:216
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CSC(C1(CO1)C2=CC=CC=C2)(F)F
Technology Process of Oxirane, 2-[difluoro(methylthio)methyl]-2-phenyl-

There total 4 articles about Oxirane, 2-[difluoro(methylthio)methyl]-2-phenyl- 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:
trimethylsulfoxonium iodide; With sodium hydride; In tetrahydrofuran; dimethyl sulfoxide; at 20 ℃; for 1h;
2,2-difluoro-2-(methylthio)acetophenone; In tetrahydrofuran; dimethyl sulfoxide; at 0 ℃; for 1h;
DOI:10.1248/cpb.49.173
Guidance literature:
Multi-step reaction with 2 steps
1.1: 49 percent / dimethylsulfoxide / 15 h / 20 °C
2.1: NaH / dimethylsulfoxide; tetrahydrofuran / 1 h / 20 °C
2.2: 95 percent / dimethylsulfoxide; tetrahydrofuran / 1 h / 0 °C
With sodium hydride; In tetrahydrofuran; dimethyl sulfoxide;
DOI:10.1248/cpb.49.173
Guidance literature:
Multi-step reaction with 3 steps
1.1: 73 percent / dimethylsulfoxide / 15 h / 20 °C
2.1: 82 percent / N-fluoro-2,4,6-trimethylpyridinium triflate; zinc bromide / 1,1,2-trichloro-ethane / 80 - 105 °C
3.1: NaH / dimethylsulfoxide; tetrahydrofuran / 1 h / 20 °C
3.2: 95 percent / dimethylsulfoxide; tetrahydrofuran / 1 h / 0 °C
With sodium hydride; 1-fluoro-2,4,6-trimethylpyridinium trifluoromethanesulfonate; zinc dibromide; In tetrahydrofuran; 1,1,2-trichloroethane; dimethyl sulfoxide;
DOI:10.1248/cpb.49.173
Refernces Edit
Post RFQ for Price