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(Z) 1-(t-butoxydiphenylsilyloxy) 6-iodo-3-butene

Base Information Edit
  • Chemical Name:(Z) 1-(t-butoxydiphenylsilyloxy) 6-iodo-3-butene
  • CAS No.:131138-01-7
  • Molecular Formula:C22H29IOSi
  • Molecular Weight:464.462
  • Hs Code.:
  • Mol file:131138-01-7.mol
(Z) 1-(t-butoxydiphenylsilyloxy) 6-iodo-3-butene

Synonyms:(Z) 1-(t-butoxydiphenylsilyloxy) 6-iodo-3-butene

Suppliers and Price of (Z) 1-(t-butoxydiphenylsilyloxy) 6-iodo-3-butene
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of (Z) 1-(t-butoxydiphenylsilyloxy) 6-iodo-3-butene Edit
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Technology Process of (Z) 1-(t-butoxydiphenylsilyloxy) 6-iodo-3-butene

There total 5 articles about (Z) 1-(t-butoxydiphenylsilyloxy) 6-iodo-3-butene 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 3 steps
1: 1) LiNH2/NH3 / 1) hexane, 2) 5h
2: 97 percent / H2 / Ni(OAc)2*4H2O, NaBH4 / ethanol / 0.25 h / 760 Torr
3: 1) MsCl, NEt3, 2) NaI / 1) CH2Cl2, RT, 0.5h, 2) acetone, 2h, reflux
With lithium amide; ammonia; hydrogen; methanesulfonyl chloride; triethylamine; sodium iodide; sodium tetrahydroborate; nickel diacetate; In ethanol;
DOI:10.1016/S0040-4020(01)96002-8
Guidance literature:
Multi-step reaction with 2 steps
1: 97 percent / H2 / Ni(OAc)2*4H2O, NaBH4 / ethanol / 0.25 h / 760 Torr
2: 1) MsCl, NEt3, 2) NaI / 1) CH2Cl2, RT, 0.5h, 2) acetone, 2h, reflux
With hydrogen; methanesulfonyl chloride; triethylamine; sodium iodide; sodium tetrahydroborate; nickel diacetate; In ethanol;
DOI:10.1016/S0040-4020(01)96002-8
Guidance literature:
Multi-step reaction with 4 steps
1: 98 percent / imidazole / dimethylformamide / 8 h / Ambient temperature
2: 1) LiNH2/NH3 / 1) hexane, 2) 5h
3: 97 percent / H2 / Ni(OAc)2*4H2O, NaBH4 / ethanol / 0.25 h / 760 Torr
4: 1) MsCl, NEt3, 2) NaI / 1) CH2Cl2, RT, 0.5h, 2) acetone, 2h, reflux
With 1H-imidazole; lithium amide; ammonia; hydrogen; methanesulfonyl chloride; triethylamine; sodium iodide; sodium tetrahydroborate; nickel diacetate; In ethanol; N,N-dimethyl-formamide;
DOI:10.1016/S0040-4020(01)96002-8
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