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Cyclofenil

Basic information Safety Supplier Related

Cyclofenil Basic information

Product Name:
Cyclofenil
Synonyms:
  • 4-((4-(acetyloxy)phenyl)cyclohexylidenemethyl)-phenoacetate
  • alpha-cyclohexylidene-alpha-(p-hydroxyphenyl)-p-cresodiacetate
  • bis-(p-acetoxyphenyl)-cyclohexylidenemethane
  • bis-(p-hydroxyphenyl)-cyclohexylidenemethanediacetate
  • cyclofenyl
  • cyclophenil
  • cyclophenyl
  • f6066
CAS:
2624-43-3
MF:
C23H24O4
MW:
364.44
EINECS:
220-089-1
Product Categories:
  • Aromatics
  • Intermediates & Fine Chemicals
  • Pharmaceuticals
Mol File:
2624-43-3.mol
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Cyclofenil Chemical Properties

Melting point:
135-136°
Boiling point:
415.62°C (rough estimate)
Density 
1.0986 (rough estimate)
refractive index 
1.4433 (estimate)
storage temp. 
2-8°C
solubility 
DMSO: 10 mg/mL at 60 °C, soluble
form 
solid
color 
White to Off-White
CAS DataBase Reference
2624-43-3(CAS DataBase Reference)
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Safety Information

WGK Germany 
2
RTECS 
GO7550000
Toxicity
LD50 oral in rat: > 12gm/kg

MSDS

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Cyclofenil Usage And Synthesis

Chemical Properties

White Solid

Originator

Ondogyne,Roussel,France,1970

Uses

Cyclofenil is a weak nonsteroidal estrogen with ovulation induction properties. Mammalian hormone.

Definition

ChEBI: Cyclofenil is an organic molecular entity.

Manufacturing Process

(A) Preparation of p-Hydroxy-p'-Methoxybenzhydrylidenecyclohexane: To a Grignard solution prepared from 110 g of magnesium (4.5 mols) and 840 g of p-bromoanisole (4.5 mols) in one liter of anhydrous ether, there was added dropwise with vigorous agitation 307 g of p-hydroxyphenyl cyclohexyl ketone (1.5 mols) dissolved in one liter of anhydrous ether. Upon completion of the addition the reaction mixture was refluxed for 2.5 hours with agitation, and was then cooled. Thereupon 15 mols of ammonium chloride dissolved in 3 liters of water were added. The ethereal layer was separated, washed with water, dried over anhydrous sodium sulfate and distilled. Yield: 370 g. BP 180° to 190°C at 0.1 mm. The substance was recrystallized from a mixture of carbon tetrachloride and petroleum ether. MP 145° to 146°C.
(B)Preparation of p,p'-Dihydroxybenzhydrylidenecyclohexane: A mixture of 118 g of p-hydroxy-p'-methoxybenzhydrylidenecyclohexane (0.4 mol), 120 g of potassium hydroxide pellets and 500 ml of triethylene glycol was stirred 4 hours at 220°C. When the reaction mixture was poured into water the substance crystallized, and the crystals were filtered off and washed with water. The substance was then recrystallized from a mixture of ethanol and petroleum ether. Yield: 104 g. MP 235° to 236°C.
(C) Preparation of p,p'-Diacetoxybenzhydrylidenecyclohexane: 56 g of p,p'- dihydroxybenzhydrylidenecyclohexane (0.2 mol) was mixed with 250 ml of acetic anhydride and 500 ml of pyridine. The mixture was refluxed for 2 hours and was then poured into water, the substance crystallizing out. The crystals were filtered off and washed with water. Finally the substance was recrystallized from ethanol. Yield: 62 g. MP 135° to 136°C.

Therapeutic Function

Ovulation stimulant

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