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23-oxa-25-hydroxyvitamin D3

Base Information
  • Chemical Name:23-oxa-25-hydroxyvitamin D3
  • CAS No.:84927-61-7
  • Molecular Formula:C26H42O3
  • Molecular Weight:402.618
  • Hs Code.:
23-oxa-25-hydroxyvitamin D<sub>3</sub>

Synonyms:

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Chemical Property of 23-oxa-25-hydroxyvitamin D3
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Technology Process of 23-oxa-25-hydroxyvitamin D3

There total 15 articles about 23-oxa-25-hydroxyvitamin 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 8 steps
1: 73 percent / potassium permanganate / H2O; ethanol / 1.) -10 deg C, 1 h, 2.) to 40 deg C, 10 min
2: 86 percent / imidazole / dimethylformamide / 2 h / Ambient temperature
3: 1.) lead tetraacetate, 2.) Red-Al / 1.) benzene, pyridine, 25 deg C, 10 min, 2.) water, 1,5h
4: 91 percent / N-chlorosuccinimide, dimethyl sulfide / 1.) CH2Cl2, -20 deg C, 30 min, 2.) 0 deg C, 30 min
5: 1.) n-butyllithium, 2.) 5percent H2O2 / 1.) hexane, THF,-50 deg C, 15 min, 2.) chloroform, 1 min
6: 73 percent / n-butyllithium / tetrahydrofuran / 1.25 h / -78 deg C to room temp.
7: 61 percent / tetra-n-butylammonium fluoride / tetrahydrofuran / 2 h / Ambient temperature
8: 1.) mercuric acetate, 2.) 3M NaOH, sodium borohydride / 1.) THF, water, 0 deg C, 2.25 h
With 1H-imidazole; lead(IV) acetate; sodium hydroxide; sodium tetrahydroborate; potassium permanganate; N-chloro-succinimide; n-butyllithium; dimethylsulfide; mercury(II) diacetate; tetrabutyl ammonium fluoride; dihydrogen peroxide; sodium bis(2-methoxyethoxy)aluminium dihydride; In tetrahydrofuran; ethanol; water; N,N-dimethyl-formamide;
DOI:10.1021/jo00157a004
Guidance literature:
Multi-step reaction with 5 steps
1: n-butyllithium / 1.) THF, hexane, 0 deg C, 2.) DMF, 75 to 78 deg C, 1.5h
2: 1.) mercuric acetate, 2.) 3M NaOH, sodium borohydride / 1.) water, THF, room temp., 1h
3: 79 percent / pyridinium trifluoroacetate, pyridinium dichromate / CH2Cl2 / 4 h / Ambient temperature
4: 98 percent / tetrahydrofuran / 2 h / Ambient temperature
5: 1.) n-butyllithium, 2.) tetra-n-butylammonium fluoride / 1.) THF, -78 deg C to room temp., 2.) THF, room temp., 2 h
With sodium hydroxide; sodium tetrahydroborate; dipyridinium dichromate; n-butyllithium; mercury(II) diacetate; tetrabutyl ammonium fluoride; pyridinium trifluroacetate; In tetrahydrofuran; dichloromethane;
DOI:10.1021/jo00157a004
Guidance literature:
Multi-step reaction with 4 steps
1: 72 percent / imidazole / dimethylformamide
2: 73 percent / n-butyllithium / tetrahydrofuran / 1.25 h / -78 deg C to room temp.
3: 61 percent / tetra-n-butylammonium fluoride / tetrahydrofuran / 2 h / Ambient temperature
4: 1.) mercuric acetate, 2.) 3M NaOH, sodium borohydride / 1.) THF, water, 0 deg C, 2.25 h
With 1H-imidazole; sodium hydroxide; sodium tetrahydroborate; n-butyllithium; mercury(II) diacetate; tetrabutyl ammonium fluoride; In tetrahydrofuran; N,N-dimethyl-formamide;
DOI:10.1021/jo00157a004
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