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(1S,2R,3S,5R)-3-(tert-butyldiphenylsilanyloxy)-5-(-6-chloropurin-9-yl)-2-fluorocyclopentanol

Base Information
  • Chemical Name:(1S,2R,3S,5R)-3-(tert-butyldiphenylsilanyloxy)-5-(-6-chloropurin-9-yl)-2-fluorocyclopentanol
  • CAS No.:902118-83-6
  • Molecular Formula:C26H28ClFN4O2Si
  • Molecular Weight:511.071
  • Hs Code.:
(1S,2R,3S,5R)-3-(tert-butyldiphenylsilanyloxy)-5-(-6-chloropurin-9-yl)-2-fluorocyclopentanol

Synonyms:(1S,2R,3S,5R)-3-(tert-butyldiphenylsilanyloxy)-5-(-6-chloropurin-9-yl)-2-fluorocyclopentanol

Suppliers and Price of (1S,2R,3S,5R)-3-(tert-butyldiphenylsilanyloxy)-5-(-6-chloropurin-9-yl)-2-fluorocyclopentanol
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Chemical Property of (1S,2R,3S,5R)-3-(tert-butyldiphenylsilanyloxy)-5-(-6-chloropurin-9-yl)-2-fluorocyclopentanol
Chemical Property:
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MSDS Files:
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Technology Process of (1S,2R,3S,5R)-3-(tert-butyldiphenylsilanyloxy)-5-(-6-chloropurin-9-yl)-2-fluorocyclopentanol

There total 5 articles about (1S,2R,3S,5R)-3-(tert-butyldiphenylsilanyloxy)-5-(-6-chloropurin-9-yl)-2-fluorocyclopentanol 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
1.1: 88 percent / N-methylmorpholine N-oxide; OsO4 / tetrahydrofuran; H2O; acetone / 24 h / 20 °C
2.1: dibutyltin oxide / benzene / 3 h / Heating
2.2: 74 percent / tetrabutylammonium bromide / benzene / 3 h / Heating
3.1: 73 percent / diethylaminosulfur trifluoride / CH2Cl2 / -78 - 20 °C
4.1: 70 percent / ceric ammonium nitrate / acetonitrile; H2O / 20 h / 20 °C
With osmium(VIII) oxide; ammonium cerium(IV) nitrate; diethylamino-sulfur trifluoride; di(n-butyl)tin oxide; 4-methylmorpholine N-oxide; In tetrahydrofuran; dichloromethane; water; acetone; acetonitrile; benzene;
DOI:10.1016/j.bmc.2006.03.011
Guidance literature:
Multi-step reaction with 3 steps
1.1: dibutyltin oxide / benzene / 3 h / Heating
1.2: 74 percent / tetrabutylammonium bromide / benzene / 3 h / Heating
2.1: 73 percent / diethylaminosulfur trifluoride / CH2Cl2 / -78 - 20 °C
3.1: 70 percent / ceric ammonium nitrate / acetonitrile; H2O / 20 h / 20 °C
With ammonium cerium(IV) nitrate; diethylamino-sulfur trifluoride; di(n-butyl)tin oxide; In dichloromethane; water; acetonitrile; benzene;
DOI:10.1016/j.bmc.2006.03.011
Guidance literature:
Multi-step reaction with 2 steps
1: 73 percent / diethylaminosulfur trifluoride / CH2Cl2 / -78 - 20 °C
2: 70 percent / ceric ammonium nitrate / acetonitrile; H2O / 20 h / 20 °C
With ammonium cerium(IV) nitrate; diethylamino-sulfur trifluoride; In dichloromethane; water; acetonitrile;
DOI:10.1016/j.bmc.2006.03.011
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