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9,11-Epoxy-16-methylpregna-1,4-dien-17-ol-3,20-dione

Base Information Edit
  • Chemical Name:9,11-Epoxy-16-methylpregna-1,4-dien-17-ol-3,20-dione
  • CAS No.:37413-99-3
  • Molecular Formula:C22H28 O4
  • Molecular Weight:356.462
  • Hs Code.:
  • Mol file:37413-99-3.mol
9,11-Epoxy-16-methylpregna-1,4-dien-17-ol-3,20-dione

Synonyms:9,11b-Epoxy-17-hydroxy-16b-methyl-9b-pregna-1,4-diene-3,20-dione

Suppliers and Price of 9,11-Epoxy-16-methylpregna-1,4-dien-17-ol-3,20-dione
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • 9β,11β-Epoxy-21dehydroxyBetamethasone
  • 50mg
  • $ 165.00
Total 2 raw suppliers
Chemical Property of 9,11-Epoxy-16-methylpregna-1,4-dien-17-ol-3,20-dione Edit
Chemical Property:
  • PSA:66.90000 
  • LogP:2.99170 
Purity/Quality:

HPLC≥98% *data from raw suppliers

9β,11β-Epoxy-21dehydroxyBetamethasone *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Uses 9β,11β-Epoxy-21dehydroxy betamethasone is synthesized from 9β,11β-epoxy-17,21-dihydroxy-16β-methylpregna-1,4-diene-3,20-dione (E589175), which is a metabolite of momestasone furoate (M490000).
Technology Process of 9,11-Epoxy-16-methylpregna-1,4-dien-17-ol-3,20-dione

There total 10 articles about 9,11-Epoxy-16-methylpregna-1,4-dien-17-ol-3,20-dione 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:
16β-methyl-17α-hydroxy-pregna-1,4,9(11)-triene-3,20-dione; With perchloric acid; 1,3-dibromo-5,5-dimethylimidazolidine-2,4-dione; In N,N-dimethyl-formamide; for 3h; cooling;
With sodium hydroxide; In methanol; dichloromethane; water; for 2h; cooling;
DOI:10.1080/00397910500464855
Guidance literature:
Multi-step reaction with 5 steps
1.1: 95 percent / pyridine / 20 °C
2.1: 70 percent / triethyl orthoformate; p-toluenesulfonic acid / CH2Cl2 / 20 h / 20 °C
3.1: 72 percent / tetrahydrofuran; diethyl ether / 72 h / 60 °C
4.1: m-iodoxybenzoic acid; diphenyl diselenide / toluene / 22 h / Heating
4.2: 50 percent / p-toluenesulfonic acid / CH2Cl2 / 4 h / 20 °C
5.1: perchloric acid; 1,3-dibromo-5,5-dimethylhydantoin / dimethylformamide / 3 h / cooling
5.2: 75.8 percent / sodium hydroxide / CH2Cl2; methanol; H2O / 2 h / cooling
With pyridine; perchloric acid; 1,3-dibromo-5,5-dimethylimidazolidine-2,4-dione; 3-iodosylbenzoic acid; diphenyl diselenide; toluene-4-sulfonic acid; orthoformic acid triethyl ester; In tetrahydrofuran; diethyl ether; dichloromethane; N,N-dimethyl-formamide; toluene;
DOI:10.1080/00397910500464855
Guidance literature:
Multi-step reaction with 2 steps
1.1: m-iodoxybenzoic acid; diphenyl diselenide / toluene / 22 h / Heating
1.2: 50 percent / p-toluenesulfonic acid / CH2Cl2 / 4 h / 20 °C
2.1: perchloric acid; 1,3-dibromo-5,5-dimethylhydantoin / dimethylformamide / 3 h / cooling
2.2: 75.8 percent / sodium hydroxide / CH2Cl2; methanol; H2O / 2 h / cooling
With perchloric acid; 1,3-dibromo-5,5-dimethylimidazolidine-2,4-dione; 3-iodosylbenzoic acid; diphenyl diselenide; In N,N-dimethyl-formamide; toluene;
DOI:10.1080/00397910500464855
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