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21-Acetyloxy DeschloroMoMetasone Furoate

Base Information Edit
  • Chemical Name:21-Acetyloxy DeschloroMoMetasone Furoate
  • CAS No.:83897-05-6
  • Molecular Formula:C29H33ClO8
  • Molecular Weight:545.029
  • Hs Code.:
  • Mol file:83897-05-6.mol
21-Acetyloxy DeschloroMoMetasone Furoate

Synonyms:

Suppliers and Price of 21-Acetyloxy DeschloroMoMetasone Furoate
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
  • Usbiological
  • 21-Acetyloxy Deschloromometasone Furoate
  • 5mg
  • $ 460.00
  • TRC
  • 21-AcetyloxyDeschloromometasoneFuroate
  • 50mg
  • $ 1320.00
  • Medical Isotopes, Inc.
  • 21-AcetyloxyDeschloromometasoneFuroate
  • 50 mg
  • $ 2200.00
Total 2 raw suppliers
Chemical Property of 21-Acetyloxy DeschloroMoMetasone Furoate Edit
Chemical Property:
  • Solubility.:Dichloromethane, Ethyl Acetate 
Purity/Quality:

HPLC≥98% *data from raw suppliers

21-Acetyloxy Deschloromometasone Furoate *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Uses 21-Acetyloxy Deschloromometasone Furoate is used in the preparation of series of novel topical corticosteroids.
Technology Process of 21-Acetyloxy DeschloroMoMetasone Furoate

There total 7 articles about 21-Acetyloxy DeschloroMoMetasone Furoate 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 hydrogenchloride; In acetic acid; for 45h;
DOI:10.1021/jm00392a010
Guidance literature:
With perchloric acid; 1,3-dichloro-5,5-dimethylhydantoin; In tetrahydrofuran; for 4h; Ambient temperature;
DOI:10.1021/jm00392a010
Guidance literature:
Multi-step reaction with 2 steps
1: 58 percent / 4-(dimethylamino)pyridine (4-DMAP) / CH2Cl2 / 144 h / Ambient temperature
2: 92 percent / HCl / acetic acid / 45 h
With hydrogenchloride; dmap; In dichloromethane; acetic acid;
DOI:10.1021/jm00392a010
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