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(2Z,6E)-<6-2H>-1-((tert-butyldiphenylsilyl)oxy)-3,7-dimethyl-2,6-nonadien-9-ol

Base Information
  • Chemical Name:(2Z,6E)-<6-2H>-1-((tert-butyldiphenylsilyl)oxy)-3,7-dimethyl-2,6-nonadien-9-ol
  • CAS No.:145208-23-7
  • Molecular Formula:C27H38O2Si
  • Molecular Weight:423.675
  • Hs Code.:
(2Z,6E)-<6-2H>-1-((tert-butyldiphenylsilyl)oxy)-3,7-dimethyl-2,6-nonadien-9-ol

Synonyms:(2Z,6E)-<6-2H>-1-((tert-butyldiphenylsilyl)oxy)-3,7-dimethyl-2,6-nonadien-9-ol

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Chemical Property of (2Z,6E)-<6-2H>-1-((tert-butyldiphenylsilyl)oxy)-3,7-dimethyl-2,6-nonadien-9-ol
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Technology Process of (2Z,6E)-<6-2H>-1-((tert-butyldiphenylsilyl)oxy)-3,7-dimethyl-2,6-nonadien-9-ol

There total 8 articles about (2Z,6E)-<6-2H>-1-((tert-butyldiphenylsilyl)oxy)-3,7-dimethyl-2,6-nonadien-9-ol 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 7 steps
1: 95 percent / imidazole / dimethylformamide; CH2Cl2 / 3 h / Ambient temperature
2: 98 percent / Na2CO3, m-chloroperbenzoic acid / CHCl3; diethyl ether / 7 h / -78 - -10 °C
3: 63 percent / periodic acid / diethyl ether / 5 h / -10 °C
4: 99 percent / piridinium dichromate / dimethylformamide / 4 °C
5: 94 percent / lithium aluminium deuteride / diethyl ether / 3 h / -10 °C
6: oxalyl chloride, dimethyl sulfoxide, triethylamine / CH2Cl2 / 2 h / -78 °C
7: 1.) nBuLi, 3.) nBuLi
With 1H-imidazole; dipyridinium dichromate; n-butyllithium; lithium aluminium deuteride; oxalyl dichloride; sodium carbonate; dimethyl sulfoxide; periodic acid; triethylamine; 3-chloro-benzenecarboperoxoic acid; In diethyl ether; dichloromethane; chloroform; N,N-dimethyl-formamide;
Guidance literature:
Multi-step reaction with 4 steps
1: 99 percent / piridinium dichromate / dimethylformamide / 4 °C
2: 94 percent / lithium aluminium deuteride / diethyl ether / 3 h / -10 °C
3: oxalyl chloride, dimethyl sulfoxide, triethylamine / CH2Cl2 / 2 h / -78 °C
4: 1.) nBuLi, 3.) nBuLi
With dipyridinium dichromate; n-butyllithium; lithium aluminium deuteride; oxalyl dichloride; dimethyl sulfoxide; triethylamine; In diethyl ether; dichloromethane; N,N-dimethyl-formamide;
Guidance literature:
Multi-step reaction with 6 steps
1: 98 percent / Na2CO3, m-chloroperbenzoic acid / CHCl3; diethyl ether / 7 h / -78 - -10 °C
2: 63 percent / periodic acid / diethyl ether / 5 h / -10 °C
3: 99 percent / piridinium dichromate / dimethylformamide / 4 °C
4: 94 percent / lithium aluminium deuteride / diethyl ether / 3 h / -10 °C
5: oxalyl chloride, dimethyl sulfoxide, triethylamine / CH2Cl2 / 2 h / -78 °C
6: 1.) nBuLi, 3.) nBuLi
With dipyridinium dichromate; n-butyllithium; lithium aluminium deuteride; oxalyl dichloride; sodium carbonate; dimethyl sulfoxide; periodic acid; triethylamine; 3-chloro-benzenecarboperoxoic acid; In diethyl ether; dichloromethane; chloroform; N,N-dimethyl-formamide;
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