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<(2S,3S)-2-(benzyloxy)-8-hydroxynon-3-yl>-p-toluenesulfonate

Base Information Edit
  • Chemical Name:<(2S,3S)-2-(benzyloxy)-8-hydroxynon-3-yl>-p-toluenesulfonate
  • CAS No.:194783-32-9
  • Molecular Formula:C23H32O5S
  • Molecular Weight:420.57
  • Hs Code.:
  • Mol file:194783-32-9.mol
<(2S,3S)-2-(benzyloxy)-8-hydroxynon-3-yl>-p-toluenesulfonate

Synonyms:<(2S,3S)-2-(benzyloxy)-8-hydroxynon-3-yl>-p-toluenesulfonate

Suppliers and Price of <(2S,3S)-2-(benzyloxy)-8-hydroxynon-3-yl>-p-toluenesulfonate
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of <(2S,3S)-2-(benzyloxy)-8-hydroxynon-3-yl>-p-toluenesulfonate Edit
Chemical Property:
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Technology Process of <(2S,3S)-2-(benzyloxy)-8-hydroxynon-3-yl>-p-toluenesulfonate

There total 5 articles about <(2S,3S)-2-(benzyloxy)-8-hydroxynon-3-yl>-p-toluenesulfonate 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 lithium aluminium tetrahydride; In tetrahydrofuran; diethyl ether; for 1h; Ambient temperature;
DOI:10.1021/jm00048a020
Guidance literature:
Multi-step reaction with 4 steps
1: 96 percent / Li2CuCl4 / diethyl ether / 1 h / -78 °C
2: 97 percent / pyridine / 12 h / Ambient temperature
3: 99 percent / 85percent m-chloroperbenzoic acid / CH2Cl2 / Ambient temperature
4: 95 percent / 1 M LAH / tetrahydrofuran; diethyl ether / 1 h / Ambient temperature
With pyridine; lithium aluminium tetrahydride; dilithium tetrachlorocuprate; 3-chloro-benzenecarboperoxoic acid; In tetrahydrofuran; diethyl ether; dichloromethane;
DOI:10.1021/jm00048a020
Guidance literature:
Multi-step reaction with 4 steps
1: 96 percent / Li2CuCl4 / diethyl ether / 1 h / -78 °C
2: 97 percent / pyridine / 12 h / Ambient temperature
3: 99 percent / 85percent m-chloroperbenzoic acid / CH2Cl2 / Ambient temperature
4: 95 percent / 1 M LAH / tetrahydrofuran; diethyl ether / 1 h / Ambient temperature
With pyridine; lithium aluminium tetrahydride; dilithium tetrachlorocuprate; 3-chloro-benzenecarboperoxoic acid; In tetrahydrofuran; diethyl ether; dichloromethane;
DOI:10.1021/jm00048a020
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