ChemicalBook > CAS DataBase List > Fluanisone

Fluanisone

Product Name
Fluanisone
CAS No.
1480-19-9
Chemical Name
Fluanisone
Synonyms
R 2028;R 2167;2028 Md;MD 2028;Fluanison;Anti-pica;Sedalande;Fluanisone;Haloanison;NSC 170977
CBNumber
CB7875027
Molecular Formula
C21H25FN2O2
Formula Weight
356.43
MOL File
1480-19-9.mol
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Fluanisone Property

Melting point:
67.5-68.5°
Boiling point:
511.8±50.0 °C(Predicted)
Density 
1.146
storage temp. 
Refrigerator
solubility 
Chloroform (Slightly), Methanol (Slightly)
pka
7.43±0.10(Predicted)
form 
Solid
color 
Off-White to Pale Yellow
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Safety

Toxicity
LD50 i.p. in mice: 200 mg/kg (Cascio)
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

Usbiological
Product number
012092
Product name
Fluanisone
Packaging
50mg
Price
$460
Updated
2021/12/16
TRC
Product number
F406800
Product name
Fluanisone
Packaging
1g
Price
$1420
Updated
2021/12/16
TRC
Product number
F406800
Product name
Fluanisone
Packaging
2g
Price
$2605
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
API0015262
Product name
FLUANISONE
Purity
95.00%
Packaging
5MG
Price
$496.31
Updated
2021/12/16
Medical Isotopes, Inc.
Product number
58057
Product name
Fluanisone
Packaging
50mg
Price
$650
Updated
2021/12/16
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Fluanisone Chemical Properties,Usage,Production

Originator

Sedalande ,J and J

Uses

Fluanisone is a butyrophenone derivative with sedative properties. It is a typical antipsychotic and is used in the treatment of schizophrenia.

Uses

Fluanisone is a neuroleptic with sedative properties and relatively poorly expressed antipsychotic action. It is used as an independent or adjuvant drug for psychomotor excitement in severe and chronic schizophrenia and for manic-depressive disorder.

Definition

ChEBI: Fluanisone is an aromatic ketone.

Manufacturing Process

To a suspension of 341 parts of aluminum chloride in 1740 parts of carbon disulfide are added 96 parts of fluorobenzene with stirring and cooling. While the temperature is maintained at about 10°C, 141 parts of γ-chlorobutyryl chloride are added. After the addition is completed, the cooling bath is removed and the stirring is continued for 2 hours. The reaction mixture is poured into ice water. The organic layer is separated, washed with water, dried over anhydrous sodium sulfate, and filtered. The filtrate is concentrated under reduced pressure, and the residue is distilled to yield γ-chloro-p-fluorobutyrophenone boiling at about 136°-142°C/6 mm
A mixture of 6.6 parts of γ-chloro-p-fluoro-butyrophenone and 12.5 parts of 1- (o-anisyl)piperazine is heated for 10 hours at a temperature of 110°C. The reaction mixture is treated with 800 parts of ether and filtered. The ether layer is washed with water, dried over anhydrous potassium carbonate and filtered, whereupon hydrogen chloride gas is introduced into the solution. The precipitate is collected on a filter and dissolved in a mixture of 240 parts of 2- propanol and 80 parts of acetone to yield 1-[γ-(p-fluorobenzoyl)propyl]-4-(o-anisyl)piperazine hydrochloride. This monohydrochloride is collected on a filter and dissolved in 240 parts of 2-propanol. Anhydrous, gaseous hydrogen chloride is passed through the solution. On cooling, the 1-[γ-(p-fluorobenzoyl) propyl]-4-(o-anisyl)piperazine dihydrochloride precipitates.
A second crop of product is obtained by passing hydrogen chloride gas through the solution of mother liquors. The pale-brown, amorphous powder is collected on a filter and found to melt at about 205°-205.5°C.
This salt is dissolved in water and treated with sodium hydroxide. The precipitated base is recovered by filtration and recrystallized from diisopropyl ether. The white crystals melt at about 67.5°-68.5°C.

Therapeutic Function

Neuroleptic

Synthesis

Fluanisone, 4??-fluoro-4-[4-(o-methoxyphenyl)-1-piperazinyl]-butyrophenone (6.3.12), is synthesized by reacting 1-(2??-methoxyphenyl)-piperazine with 4-chloro- 4??-fluorobutyrophenone (6.3.4) [50].

Fluanisone Preparation Products And Raw materials

Raw materials

Preparation Products

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View Lastest Price from Fluanisone manufacturers

Shaanxi Franta Biotechnology Co., Ltd
Product
fluanisone 1480-19-9
Price
US $20.00/kg
Min. Order
1kg
Purity
99
Supply Ability
1000kg
Release date
2024-03-27
Xiamen Wonderful Bio Technology Co., Ltd.
Product
fluanisone 1480-19-9
Price
US $15.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
large quantity
Release date
2023-07-21
Hebei Yanxi Chemical Co., Ltd.
Product
Fluanisone 1480-19-9
Price
US $50.00/kg
Min. Order
1kg
Purity
0.99
Supply Ability
10000
Release date
2023-09-08

1480-19-9, FluanisoneRelated Search:


  • Fluanisone
  • 1-Butanone, 1-(4-fluorophenyl)-4-4-(2-methoxyphenyl)-1-piperazinyl-
  • 2028 Md
  • 4-[4-(o-Methoxyphenyl)-1-piperazinyl]-p-fluorobutyrophenone
  • 4'-Fluoro-4-[4-(o-methoxyphenyl)-1-piperazinyl]butyrophenone
  • Anti-pica
  • Butyrophenone, 4'-fluoro-4-[4-(o-methoxyphenyl)-1-piperazinyl]-
  • Fluanison
  • Haloanison
  • 1-(4-Fluorophenyl)-4-[4-(2-methoxyphenyl)-1-piperazinyl]-1-butanone
  • Haloanisone
  • MD 2028
  • NSC 170977
  • p-Fluoro-γ-[4-(o-Methoxyphenyl)-1-piperazinyl]butyrophenone
  • R 2028
  • R 2167
  • Sedalande
  • γ-(4-o-Methoxyphenylpiperazino)-4-fluorobutyrophenone
  • 1-(4-fluorophenyl)-4-[4-(2-methoxyphenyl)piperazin-1-yl]butan-1-one
  • 1-(4-fluorophenyl)-4-4-(2-methoxyphenyl)-1-piperazinyl
  • Flusnisone
  • Fluanisone USP/EP/BP
  • 1480-19-9
  • C21H25FN2O2
  • Aromatics
  • Heterocycles
  • Intermediates & Fine Chemicals
  • Neurochemicals
  • Pharmaceuticals