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14-epi-2α-methyl-1α,25-dihydroxy-19-nortachysterol

Base Information
  • Chemical Name:14-epi-2α-methyl-1α,25-dihydroxy-19-nortachysterol
  • CAS No.:1298076-01-3
  • Molecular Formula:C27H44O3
  • Molecular Weight:416.645
  • Hs Code.:
14-epi-2α-methyl-1α,25-dihydroxy-19-nortachysterol

Synonyms:14-epi-2α-methyl-1α,25-dihydroxy-19-nortachysterol

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Chemical Property of 14-epi-2α-methyl-1α,25-dihydroxy-19-nortachysterol
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Technology Process of 14-epi-2α-methyl-1α,25-dihydroxy-19-nortachysterol

There total 20 articles about 14-epi-2α-methyl-1α,25-dihydroxy-19-nortachysterol 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 Wilkinson's catalyst; hydrogen; In dichloromethane; benzene; at 20 ℃; for 1h; regioselective reaction;
DOI:10.1021/ja201481j
Guidance literature:
Multi-step reaction with 6 steps
1.1: lithium diisopropyl amide / tetrahydrofuran; hexane / -78 - 20 °C / Inert atmosphere
1.2: -78 - 20 °C / Inert atmosphere
2.1: copper(l) iodide; bis(acetato)bis(triphenylphosphine)palladium(0); diethylamine / N,N-dimethyl-formamide / 1.5 h / 20 °C / Inert atmosphere
3.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 0 - 20 °C / Inert atmosphere
4.1: Wilkinson's catalyst; hydrogen / dichloromethane; benzene / 1 h / 20 °C
5.1: quinoline; hydrogen / methanol; dichloromethane / 0.25 h / 20 °C
6.1: hydrogenchloride / water
With quinoline; hydrogenchloride; copper(l) iodide; Wilkinson's catalyst; bis(acetato)bis(triphenylphosphine)palladium(0); tetrabutyl ammonium fluoride; hydrogen; diethylamine; lithium diisopropyl amide; In tetrahydrofuran; methanol; hexane; dichloromethane; water; N,N-dimethyl-formamide; benzene; 2.1: Sonogashira coupling reaction;
DOI:10.1021/ja201481j
Guidance literature:
Multi-step reaction with 7 steps
1.1: tetra-n-propylammonium perruthenate.; 4-methylmorpholine N-oxide / dichloromethane / 0 - 20 °C / Molecular sieve; Inert atmosphere
2.1: n-butyllithium / tetrahydrofuran; diethyl ether; hexane / 0.5 h / -78 °C / Inert atmosphere
2.2: 2.25 h / -78 - 0 °C / Inert atmosphere
3.1: copper(l) iodide; bis(acetato)bis(triphenylphosphine)palladium(0); diethylamine / N,N-dimethyl-formamide / 1.5 h / 20 °C / Inert atmosphere
4.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 0 - 20 °C / Inert atmosphere
5.1: Wilkinson's catalyst; hydrogen / dichloromethane; benzene / 1 h / 20 °C
6.1: quinoline; hydrogen / methanol; dichloromethane / 0.25 h / 20 °C
7.1: hydrogenchloride / water
With quinoline; hydrogenchloride; copper(l) iodide; Wilkinson's catalyst; n-butyllithium; bis(acetato)bis(triphenylphosphine)palladium(0); tetra-n-propylammonium perruthenate.; tetrabutyl ammonium fluoride; hydrogen; 4-methylmorpholine N-oxide; diethylamine; In tetrahydrofuran; methanol; diethyl ether; hexane; dichloromethane; water; N,N-dimethyl-formamide; benzene; 3.1: Sonogashira coupling reaction;
DOI:10.1021/ja201481j
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