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(22E,24R)-24,25-dihydroxy-22-dehydrovitamin D3

Base Information Edit
  • Chemical Name:(22E,24R)-24,25-dihydroxy-22-dehydrovitamin D3
  • CAS No.:112670-94-7
  • Molecular Formula:C27H42O3
  • Molecular Weight:414.629
  • Hs Code.:
  • Mol file:112670-94-7.mol
(22E,24R)-24,25-dihydroxy-22-dehydrovitamin D<sub>3</sub>

Synonyms:

Suppliers and Price of (22E,24R)-24,25-dihydroxy-22-dehydrovitamin D3
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of (22E,24R)-24,25-dihydroxy-22-dehydrovitamin D3 Edit
Chemical Property:
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Technology Process of (22E,24R)-24,25-dihydroxy-22-dehydrovitamin D3

There total 14 articles about (22E,24R)-24,25-dihydroxy-22-dehydrovitamin D3 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 5 steps
1: 39 percent / n-butyllithium, diisopropylamine / tetrahydrofuran / 3 h / -78 °C
2: 90 percent / p-toluenesulfonic acid / benzene / 2 h / Ambient temperature
3: 1.) sodium borohydride; 2.) N,N-diisopropyl ethylamine / 1.) methanol, THF, r.t., 2 h: 2.) Ch2Cl2, r.t., 3 h
4: lithium aluminum hydride
5: 1.) ethanol, irrad., quartz cell; 2.) ref., ethanol
With sodium tetrahydroborate; lithium aluminium tetrahydride; n-butyllithium; toluene-4-sulfonic acid; diisopropylamine; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; benzene;
DOI:10.1248/cpb.35.970
Guidance literature:
Multi-step reaction with 5 steps
1: 39 percent / n-butyllithium, diisopropylamine / tetrahydrofuran / 3 h / -78 °C
2: 90 percent / p-toluenesulfonic acid / benzene / 2 h / Ambient temperature
3: 1.) sodium borohydride; 2.) N,N-diisopropyl ethylamine / 1.) methanol, THF, r.t., 2 h: 2.) Ch2Cl2, r.t., 3 h
4: lithium aluminum hydride
5: 1.) ethanol, irrad., quartz cell; 2.) ref., ethanol
With sodium tetrahydroborate; lithium aluminium tetrahydride; n-butyllithium; toluene-4-sulfonic acid; diisopropylamine; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; benzene;
DOI:10.1248/cpb.35.970
Guidance literature:
Multi-step reaction with 4 steps
1: 90 percent / p-toluenesulfonic acid / benzene / 2 h / Ambient temperature
2: 1.) sodium borohydride; 2.) N,N-diisopropyl ethylamine / 1.) methanol, THF, r.t., 2 h: 2.) Ch2Cl2, r.t., 3 h
3: lithium aluminum hydride
4: 1.) ethanol, irrad., quartz cell; 2.) ref., ethanol
With sodium tetrahydroborate; lithium aluminium tetrahydride; toluene-4-sulfonic acid; N-ethyl-N,N-diisopropylamine; In benzene;
DOI:10.1248/cpb.35.970
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