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trans,trans-(5S)-5-<9'-(2,3-bis((dimethylthexylsilyl)oxy)cyclohexyl)-3'-nonenyl>-2,3-dihydrofuranone

Base Information Edit
  • Chemical Name:trans,trans-(5S)-5-<9'-(2,3-bis((dimethylthexylsilyl)oxy)cyclohexyl)-3'-nonenyl>-2,3-dihydrofuranone
  • CAS No.:114528-96-0
  • Molecular Formula:C35H68O4Si2
  • Molecular Weight:609.094
  • Hs Code.:
  • Mol file:114528-96-0.mol
trans,trans-(5S)-5-<9'-(2,3-bis((dimethylthexylsilyl)oxy)cyclohexyl)-3'-nonenyl>-2,3-dihydrofuranone

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Chemical Property of trans,trans-(5S)-5-<9'-(2,3-bis((dimethylthexylsilyl)oxy)cyclohexyl)-3'-nonenyl>-2,3-dihydrofuranone Edit
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Technology Process of trans,trans-(5S)-5-<9'-(2,3-bis((dimethylthexylsilyl)oxy)cyclohexyl)-3'-nonenyl>-2,3-dihydrofuranone

There total 11 articles about trans,trans-(5S)-5-<9'-(2,3-bis((dimethylthexylsilyl)oxy)cyclohexyl)-3'-nonenyl>-2,3-dihydrofuranone 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:
Multi-step reaction with 4 steps
1: 85 percent / PPh3, CBr4 / acetonitrile / Ambient temperature
2: 70 percent / azobisisobutyronitryle / toluene / 30 h / Heating
3: 1. O3, 2.) Me2S / 1.) MeOH, CH2Cl2, -78 deg C, 2.) -78 deg C, 1 h
4: various solvent(s) / 40 h / Heating
With dimethylsulfide; 2,2'-azobis(isobutyronitrile); carbon tetrabromide; ozone; triphenylphosphine; In toluene; acetonitrile;
DOI:10.1021/jo00247a014
Guidance literature:
Multi-step reaction with 7 steps
1: 95 percent / Et3N, bis(trimethylsilyl)amine / tetrahydrofuran / Ambient temperature
3: 1.) BH3*Me2S, 2.) 3 N NaOH, 30percent H2O2 / 1.) THF, RT, 3 days 2.) 1 h
4: 84 percent / CBr4, PPh3 / acetonitrile / 1 h / 0 °C
5: 95 percent / lutidine / CH2Cl2 / 0 - 20 °C
6: acetonitrile / 72 h / Heating
7: various solvent(s) / 40 h / Heating
With sodium hydroxide; carbon tetrabromide; dimethylsulfide borane complex; lutidine; dihydrogen peroxide; triethylamine; triphenylphosphine; 1,1,1,3,3,3-hexamethyl-disilazane; In tetrahydrofuran; dichloromethane; acetonitrile;
DOI:10.1021/jo00247a014
Guidance literature:
Multi-step reaction with 8 steps
1: 98 percent / BH3*Me2S / tetrahydrofuran / 0 °C
2: 95 percent / Et3N, bis(trimethylsilyl)amine / tetrahydrofuran / Ambient temperature
4: 1.) BH3*Me2S, 2.) 3 N NaOH, 30percent H2O2 / 1.) THF, RT, 3 days 2.) 1 h
5: 84 percent / CBr4, PPh3 / acetonitrile / 1 h / 0 °C
6: 95 percent / lutidine / CH2Cl2 / 0 - 20 °C
7: acetonitrile / 72 h / Heating
8: various solvent(s) / 40 h / Heating
With sodium hydroxide; carbon tetrabromide; dimethylsulfide borane complex; lutidine; dihydrogen peroxide; triethylamine; triphenylphosphine; 1,1,1,3,3,3-hexamethyl-disilazane; In tetrahydrofuran; dichloromethane; acetonitrile;
DOI:10.1021/jo00247a014
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