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1-[1-benzyloxy-(1S)-ethyl]-2-tert-butyldimethylsilyloxymethyl-(1S,2S)-hexyl alcohol

Base Information Edit
  • Chemical Name:1-[1-benzyloxy-(1S)-ethyl]-2-tert-butyldimethylsilyloxymethyl-(1S,2S)-hexyl alcohol
  • CAS No.:790664-79-8
  • Molecular Formula:C22H40O3Si
  • Molecular Weight:380.643
  • Hs Code.:
  • Mol file:790664-79-8.mol
1-[1-benzyloxy-(1S)-ethyl]-2-tert-butyldimethylsilyloxymethyl-(1S,2S)-hexyl alcohol

Synonyms:1-[1-benzyloxy-(1S)-ethyl]-2-tert-butyldimethylsilyloxymethyl-(1S,2S)-hexyl alcohol

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Chemical Property of 1-[1-benzyloxy-(1S)-ethyl]-2-tert-butyldimethylsilyloxymethyl-(1S,2S)-hexyl alcohol Edit
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Technology Process of 1-[1-benzyloxy-(1S)-ethyl]-2-tert-butyldimethylsilyloxymethyl-(1S,2S)-hexyl alcohol

There total 4 articles about 1-[1-benzyloxy-(1S)-ethyl]-2-tert-butyldimethylsilyloxymethyl-(1S,2S)-hexyl alcohol 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: 85 percent / DIBAL-H / toluene; CH2Cl2 / 0.5 h / -20 °C
2.1: 71 percent / (-)-diisopropyl tartrate; titanium isopropoxide; cumene hydroperoxide / 4 Angstroem molecular sieves / CH2Cl2 / 12 h / -20 °C
3.1: copper(I) iodide / diethyl ether; hexane / 0.5 h / -20 °C
3.2: 80 percent / diethyl ether; hexane / 1 h / -20 °C
4.1: 83 percent / imidazole / CH2Cl2 / 1 h / 20 °C
With 1H-imidazole; titanium(IV) isopropylate; copper(l) iodide; (-)-diisopropyl tartrate; Cumene hydroperoxide; diisobutylaluminium hydride; 4 A molecular sieve; In diethyl ether; hexane; dichloromethane; toluene; 2.1: Sharpless asymmetric epoxidation;
DOI:10.1055/s-2004-829173
Guidance literature:
Multi-step reaction with 3 steps
1.1: 71 percent / (-)-diisopropyl tartrate; titanium isopropoxide; cumene hydroperoxide / 4 Angstroem molecular sieves / CH2Cl2 / 12 h / -20 °C
2.1: copper(I) iodide / diethyl ether; hexane / 0.5 h / -20 °C
2.2: 80 percent / diethyl ether; hexane / 1 h / -20 °C
3.1: 83 percent / imidazole / CH2Cl2 / 1 h / 20 °C
With 1H-imidazole; titanium(IV) isopropylate; copper(l) iodide; (-)-diisopropyl tartrate; Cumene hydroperoxide; 4 A molecular sieve; In diethyl ether; hexane; dichloromethane; 1.1: Sharpless asymmetric epoxidation;
DOI:10.1055/s-2004-829173
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