ChemicalBook > CAS DataBase List > Flunarizine

Flunarizine

Product Name
Flunarizine
CAS No.
52468-60-7
Chemical Name
Flunarizine
Synonyms
Sibelium;Fluarizine;FLUNARIZINE;(e)-piperazin;Flunarizine USP/EP/BP;Flunarizine Dihydrate;Flunarizine in methanol;(E)-1-[Bis-(p-fluorophenyl)methyl]-4-cinnamylpiperazine;(e)-1-[bis(4-fluorophenyl)methyl]-4-(3-phenyl-2-propenyl)piperazine;1-[Bis(4-fluorophenyl)methyl]-4-[(E)-3-phenyl-2-propenyl]piperazine
CBNumber
CB2757102
Molecular Formula
C26H26F2N2
Formula Weight
404.49
MOL File
52468-60-7.mol
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Flunarizine Property

Boiling point:
511.3±50.0 °C(Predicted)
Density 
1.170±0.06 g/cm3(Predicted)
storage temp. 
2-8°C
form 
Solid
pka
6.99±0.10(Predicted)
color 
White to off-white
CAS DataBase Reference
52468-60-7(CAS DataBase Reference)
NIST Chemistry Reference
Piperazine, 1-[bis(4-fluorophenyl)methyl]-4-(3-phenyl-2-propenyl)-, (e)-(52468-60-7)
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

American Custom Chemicals Corporation
Product number
API0002726
Product name
FLUNARIZINE
Purity
95.00%
Packaging
1G
Price
$160.65
Updated
2021/12/16
Medical Isotopes, Inc.
Product number
D33984
Product name
Flunarizine-d8dHCl
Packaging
1mg
Price
$600
Updated
2021/12/16
Medical Isotopes, Inc.
Product number
D33984
Product name
Flunarizine-d8dHCl
Packaging
5mg
Price
$1670
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
API0002726
Product name
FLUNARIZINE
Purity
95.00%
Packaging
25G
Price
$2243.59
Updated
2021/12/16
Crysdot
Product number
CD11110920
Product name
1-(Bis(4-fluorophenyl)methyl)-4-cinnamylpiperazine
Purity
95+%
Packaging
1g
Price
$84
Updated
2021/12/16
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Flunarizine Chemical Properties,Usage,Production

Description

Flunarizine is the difluorinated derivative of cinnarizine. Thus, its preparation and therapeutic use are identical to those of cinnarizine.

Originator

Sibelium,Janssen,W. Germany,1977

Uses

Vasodilator.

Definition

ChEBI: Flunarizine is a diarylmethane.

Manufacturing Process

A mixture of 14.3 parts of di-(p-fluorophenyl)-chloromethane, 10.1 parts of 1- cinnamylpiperazine, 12.7 parts of sodium carbonate, a few crystals of potassium iodide in 200 parts of 4-methyl-2-pentanone is stirred and refluxed for 21 hours. The reaction mixture is cooled and 50 parts of water are added. The organic layer is separated, dried, filtered and evaporated.
The oily residue is dissolved in 480 parts of anhydrous diisopropyl ether. This solution is boiled with activated charcoal, filtered and to the clear filtrate is added an excess of 2-propanol, previously saturated with gaseous hydrogen chloride. The precipitated salt is filtered off and recrystallized from a mixture of 2-propanol and ethanol, yielding 1-cinnamyl-4-(di-p-fluorobenzhydryl) piperazine dihydrochloride, MP 251.5°C.

Therapeutic Function

Vasodilator

World Health Organization (WHO)

Flunarizine, an antihistaminic and vasodilator agent, was introduced into medicine in 1970. It is indicated for the treatment of central and peripheral vascular disorders. However, its effectiveness in these conditions has not been convincingly demonstrated, and its use has been associated with adverse reactions involving the central nervous system, including extrapyramidal disturbances and depression. This has led several regulatory authorities to restrict the approved indications for products containing flunarizine.

Flunarizine Preparation Products And Raw materials

Raw materials

Preparation Products

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52468-60-7, FlunarizineRelated Search:


  • (E)-1-[Bis-(p-fluorophenyl)methyl]-4-cinnamylpiperazine
  • (e)-piperazin
  • 1-[Bis(4-fluorophenyl)methyl]-4-[(2E)-3-phenyl-2-propenyl]piperazine
  • Piperazine, 1-[bis(4-fluorophenyl)methyl]-4-(3-phenyl-2-propenyl)-, (E)-
  • Sibelium
  • Fluarizine
  • 1-[Bis(4-fluorophenyl)methyl]-4-[(E)-3-phenyl-2-propenyl]piperazine
  • FLUNARIZINE
  • (e)-1-[bis(4-fluorophenyl)methyl]-4-(3-phenyl-2-propenyl)piperazine
  • Piperazine, 1-[bis(4-fluorophenyl)methyl]-4-[(2E)-3-phenyl-2-propen-1-yl]-
  • Flunarizine USP/EP/BP
  • Flunarizine Dihydrate
  • Flunarizine in methanol
  • 52468-60-7
  • C26H26F2N2