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fluclorolone acetonide

CAS No.
3693-39-8
Chemical Name:
fluclorolone acetonide
Synonyms
Topilar;RS-2252;Flulorolone;Fluclorolone;Flucloronide;Flucortolone acetonide;Flucloronide (Fluclorolone Acetonide);9α,11β-Dichloro-6α-fluoro-16α,17α,21-trihydroxypregna-1,4-diene-3,20-dione-16,17-acetonide;9,11β-Dichloro-6α-fluoro-21-hydroxy-16α,17-(isopropylidenedioxy)pregna-1,4-diene-3,20-dione;9α,11β-Dichloro-6α-fluoro-21-hydroxy-16α,17α-(isopropylidenebisoxy)pregna-1,4-diene-3,20-dione
CBNumber:
CB3900941
Molecular Formula:
C24H29Cl2FO5
Molecular Weight:
487.392
MDL Number:
MFCD00200362
MOL File:
3693-39-8.mol
MSDS File:
SDS
Last updated:2023-05-04 17:34:38

fluclorolone acetonide Properties

Boiling point 598.3±50.0 °C(Predicted)
Density 1.38±0.1 g/cm3(Predicted)
pka 12.87±0.10(Predicted)
FDA UNII MG258KTA37
ATC code D07AC02

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS08
Signal word  Warning
Hazard statements  H373-H361-H362
Precautionary statements  P260-P314-P501-P201-P202-P281-P308+P313-P405-P501-P201-P260-P263-P264-P270-P308+P313

fluclorolone acetonide price More Price(3)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TRC F418900 Flucloronide 3693-39-8 2.5mg $165 2021-12-16 Buy
TRC F418900 Flucloronide 3693-39-8 25mg $1320 2021-12-16 Buy
American Custom Chemicals Corporation API0016509 FLUCLORONIDE 95.00% 3693-39-8 5MG $495.19 2021-12-16 Buy
Product number Packaging Price Buy
F418900 2.5mg $165 Buy
F418900 25mg $1320 Buy
API0016509 5MG $495.19 Buy

fluclorolone acetonide Chemical Properties,Uses,Production

Originator

Topilar,Syntex,UK,1971

Uses

fluclorolone acetonide is a synthetic glucocorticoid with anti-inflammatory properties. Studies suggest that it is a potent inhibitor of mouse skin tumor promotion and epidermal DNA synthesis.

Definition

ChEBI: Fluclorolone acetonide is a 21-hydroxy steroid.

Manufacturing Process

To 6α-fluoro-16α-hydroxy-hydrocortisone 21-acetate, described by Mills et al, J. Am. Chem. Soc., volume 81, pages 1264 to 1265, March 5, 1959, there was added acetic anhydride in dry pyridine. The reaction mixture was left at room temperature overnight and was then poured with stirring into ice water. The resulting precipitate was filtered, washed with water and crystallized from acetone-hexane to give 6α-fluoro-16α-hydroxy-hydrocortisone-16α,21- diacetate. This was reacted with methane-sulfonyl chloride in dimethyl formamide in the presence of pyridine at 80°C for 1 hour. The mixture was cooled, diluted with water and extracted with ethyl acetate. The extract was washed with water, dried over anhydrous sodium sulfate and the ethyl acetate was evaporated. By recrystallization of the residue from acetone-hexane there was obtained 6α-fluoro-Δ4,9(11)-pregnadiene-16α,17α,21-triol-3,20-dione- 16α,21-diacetate.
This was reacted with chlorine to give the dichloropregnene compound, then with selenium dioxide to give the dichloropregnadiene compound. By hydrolysis with methanolic potassium hydroxide there was obtained the free 6α-fluoro-9α,11β-dichloro-Δ1,4-pregnadiene-16α,17α,21-triol-3,20-dione. By treatment with acetone in the presence of perchloric acid, the 16,17-acetonide of 6α-fluoro-9α,11β-dichloro-Δ1,4-pregnadiene-16α,17α,21-triol-3,20-dione was formed.

Therapeutic Function

Glucocorticoid

fluclorolone acetonide Preparation Products And Raw materials

Raw materials

Preparation Products

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Flucloronide Fluclorolone Flulorolone (6α,11β,16α)-9,11-Dichloro-6-fluoro-21-hydroxy-16,17-[(1-Methylethylidene)bis(oxy)]pregna-1,4-diene-3,20-dione 9,11β-Dichloro-6α-fluoro-21-hydroxy-16α,17-(isopropylidenedioxy)pregna-1,4-diene-3,20-dione 9α,11β-Dichloro-6α-fluoro-16α,17α,21-trihydroxypregna-1,4-diene-3,20-dione-16,17-acetonide Flucortolone acetonide 9α,11β-Dichloro-6α-fluoro-21-hydroxy-16α,17α-(isopropylidenebisoxy)pregna-1,4-diene-3,20-dione RS-2252 Topilar Flucloronide (Fluclorolone Acetonide) Pregna-1,4-diene-3,20-dione, 9,11-dichloro-6-fluoro-21-hydroxy-16,17-[(1-methylethylidene)bis(oxy)]-, (6α,11β,16α)- 3693-39-8 C24H29Cl2FO5 Inhibitors Intermediates & Fine Chemicals Pharmaceuticals Steroids Inhibitors, Pharmaceuticals, Intermediates & Fine Chemicals, Steroids