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(1R,2S,3R,4S,7R)-(6-benzenesulfonyl-2,4-dimethyl-8-oxabicyclo[5.1.0]oct-5-en-3-yloxy)-tert-butyldimethylsilane

Base Information
  • Chemical Name:(1R,2S,3R,4S,7R)-(6-benzenesulfonyl-2,4-dimethyl-8-oxabicyclo[5.1.0]oct-5-en-3-yloxy)-tert-butyldimethylsilane
  • CAS No.:606128-63-6
  • Molecular Formula:C21H32O4SSi
  • Molecular Weight:408.634
  • Hs Code.:
(1R,2S,3R,4S,7R)-(6-benzenesulfonyl-2,4-dimethyl-8-oxabicyclo[5.1.0]oct-5-en-3-yloxy)-tert-butyldimethylsilane

Synonyms:(1R,2S,3R,4S,7R)-(6-benzenesulfonyl-2,4-dimethyl-8-oxabicyclo[5.1.0]oct-5-en-3-yloxy)-tert-butyldimethylsilane

Suppliers and Price of (1R,2S,3R,4S,7R)-(6-benzenesulfonyl-2,4-dimethyl-8-oxabicyclo[5.1.0]oct-5-en-3-yloxy)-tert-butyldimethylsilane
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Chemical Property of (1R,2S,3R,4S,7R)-(6-benzenesulfonyl-2,4-dimethyl-8-oxabicyclo[5.1.0]oct-5-en-3-yloxy)-tert-butyldimethylsilane
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Technology Process of (1R,2S,3R,4S,7R)-(6-benzenesulfonyl-2,4-dimethyl-8-oxabicyclo[5.1.0]oct-5-en-3-yloxy)-tert-butyldimethylsilane

There total 8 articles about (1R,2S,3R,4S,7R)-(6-benzenesulfonyl-2,4-dimethyl-8-oxabicyclo[5.1.0]oct-5-en-3-yloxy)-tert-butyldimethylsilane 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 2 steps
1: lutidine / CH2Cl2 / 2 h / 25 °C
2: Mo(CO)6; tert-butyl hydroperoxide
With tert.-butylhydroperoxide; hexacarbonyl molybdenum; lutidine; In dichloromethane;
DOI:10.1002/anie.200350955
Guidance literature:
Multi-step reaction with 6 steps
1.1: tetrahydrofuran / -78 °C
1.2: tetrahydrofuran / -78 - 20 °C
2.1: trimethylsilyl triflate; (C2H5)3N / CH2Cl2 / Heating
3.1: n-C4H9Li / tetrahydrofuran / 1.5 h / -78 - -5 °C
3.2: tetrahydrofuran / -90 - -50 °C
4.1: m-chloroperbenzoic acid / CH2Cl2 / 1 h / 25 °C
5.1: lutidine / CH2Cl2 / 2 h / 25 °C
6.1: Mo(CO)6; tert-butyl hydroperoxide
With tert.-butylhydroperoxide; n-butyllithium; hexacarbonyl molybdenum; trimethylsilyl trifluoromethanesulfonate; lutidine; triethylamine; 3-chloro-benzenecarboperoxoic acid; In tetrahydrofuran; dichloromethane;
DOI:10.1002/anie.200350955
Guidance literature:
Multi-step reaction with 4 steps
1.1: n-C4H9Li / tetrahydrofuran / 1.5 h / -78 - -5 °C
1.2: tetrahydrofuran / -90 - -50 °C
2.1: m-chloroperbenzoic acid / CH2Cl2 / 1 h / 25 °C
3.1: lutidine / CH2Cl2 / 2 h / 25 °C
4.1: Mo(CO)6; tert-butyl hydroperoxide
With tert.-butylhydroperoxide; n-butyllithium; hexacarbonyl molybdenum; lutidine; 3-chloro-benzenecarboperoxoic acid; In tetrahydrofuran; dichloromethane;
DOI:10.1002/anie.200350955
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