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4828-27-7

4828-27-7 Structure

4828-27-7 Structure
IdentificationBack Directory
[Name]

Clocortolone
[CAS]

4828-27-7
[Synonyms]

9-Chlor
Clocortolon
CLOCORTOLONE
Clocortolona
Clocortolonum
9-Chloro-6α-fluoro-11β,21-dihydroxy-16α-methylpregna-1,4-diene-3,20-dione
9-Chloro-6α-fluoro-11β,21-dihydroxy-17α-Methylpregna-1,4-diene-3,20-dione
(6α,11β,16α)-9-Chloro-6-fluoro-11,21-dihydroxy-16-Methylpregna-1,4-diene-3,20-dione
Pregna-1,4-diene-3,20-dione, 9-chloro-6-fluoro-11,21-dihydroxy-16-methyl-, (6α,11β,16α)-
Pregna-1,4-diene-3,20-dione, 9-chloro-6-fluoro-11,21-dihydroxy-16-methyl-, (6a,11b,16a)-
9-alpha-chloro-6-alpha-fluoro-11-beta,21-dihydroxy-16-alpha-methylpregna-1,4-diene-3,20-dione
(6s,9r,16r)-9-chloro-6-fluoro-11-hydroxy-17-(2-hydroxyacetyl)-10,13,16-trimethyl-7,8,11,12,14,15,16,17-octahydro-6h-cyclopenta[a]phenanthren-3-one
(6S,8S,9R,10S,11S,13S,14S,16R,17S)-9-Chloro-6-fluoro-11-hydroxy-17-(2-hydroxyacetyl)-10,13,16-trimethyl-7,8,11,12,14,15,16,17-octahydro-6H-cyclopenta[a]phenanthren-3-one
[EINECS(EC#)]

225-406-7
[Molecular Formula]

C22H28ClFO4
[MDL Number]

MFCD05662233
[MOL File]

4828-27-7.mol
[Molecular Weight]

410.91
Chemical PropertiesBack Directory
[Melting point ]

254° (dec)
[storage temp. ]

Refrigerator, Under Inert Atmosphere
[solubility ]

Chloroform (Slightly), Dioxane (Slightly), DMSO (Slightly), Methanol (Slightly)
[form ]

Solid
[color ]

White to Light Yellow
Material Safety Data Sheet(MSDS)Back Directory
[msds information]

Clocortolone(4828-27-7).msds
Hazard InformationBack Directory
[Originator]

Clocortolone,Schering AG
[Uses]

Clocortolone can be used in the treatment of skin inflammmation and other skin conditions arising for dermatoses.
[Uses]

Corticosteroid used in the treatment of skin inflammmation and other skin conditions arising for dermatoses.
[Definition]

ChEBI: Clocortolone is 16alpha-Methylpregna-1,4-diene-3,20-dione bearing hydroxy substituents at the 11beta and 21 positions, fluorine at position 6 and chlorine at position 9. A medium potency corticosteroid, it is used as its 21-O-pivalate or caproate ester for the relief of inflammatory and pruritic (itching) skin disorders. It has a role as an anti-inflammatory drug and an antipruritic drug. It is a glucocorticoid, an 11beta-hydroxy steroid, a 21-hydroxy steroid, a 20-oxo steroid, a fluorinated steroid, a 3-oxo-Delta(1),Delta(4)-steroid, a chlorinated steroid and a primary alpha-hydroxy ketone.
[Manufacturing Process]

6α-Fluoro-16α-methyl-21-hydroxy-1,4,9(11)-pregnatriene-3,20-dione is suspended in nitroethane at heating. To this suspension 1 N perchloric acid is added and then t-butyl hypochlorite is added dropwise. The reaction mixture is agitated at heating, then cooled to room temperature, mixed with methanol, stirred and then poured with water containing ice. The mixture is then stirred, thus precipitated product is filtered, washed neutral with water, dried; The crude product is treated with hot methanol, and recrystallized from ethanol, thus 9α-chloro-6α-fluoro-11β,21-dihydroxy-16α-methyl-1,4- pregnadiene-3,20-dione was obtained.
[Therapeutic Function]

Glucocorticoid
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