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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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Fluanisone Suppliers

J & K SCIENTIFIC LTD.
Tel
010-82848833 400-666-7788
Fax
86-10-82849933
Email
jkinfo@jkchemical.com
Country
China
ProdList
96815
Advantage
76
LGM Pharma
Tel
1-(800)-881-8210
Fax
615-250-9817
Email
inquiries@lgmpharma.com
Country
United States
ProdList
2123
Advantage
70
Chemsky(shanghai)International Co.,Ltd.
Tel
021-50135380
Email
shchemsky@163.com
Country
China
ProdList
283
Advantage
58
Chemsky(shanghai)International Co.,Ltd.
Tel
021-50135380
Email
shchemsky@sina.com
Country
China
ProdList
32321
Advantage
50
Nanjing Sunlida Biological Technology Co., Ltd.
Tel
025-57798810
Fax
025-57019371
Email
sales@sunlidabio.com
Country
China
ProdList
3239
Advantage
55
Shanghai Worldyang Chemical Co.,Ltd.
Tel
021-021-56795766
Fax
+86-21-56795266
Email
sales@worldyachem.com
Country
China
ProdList
9346
Advantage
58
Wuhan Dahua Pharmaceutical Co., Ltd.
Tel
027-59262863 13277907145 3091977954
Fax
027-59420980
Country
China
ProdList
4943
Advantage
58
Struchem Co., Ltd.
Tel
0512-0512-63009836 15365350169
Fax
0512-63006936
Email
helen@struchem.com
Country
China
ProdList
3984
Advantage
60
ShangHai Siyan Biological Technology Co., Ltd.
Tel
021-50908862,442785678,326799392 18721037013
Fax
021-50908862
Email
siyansales@126.com
Country
China
ProdList
9627
Advantage
58
Raw material medicin reagent co.,Ltd
Tel
Email
sales@njromanme.com
Country
China
ProdList
4529
Advantage
58
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View Lastest Price from Fluanisone manufacturers

Hebei Miaoyin Technology Co.,Ltd
Product
fluanisone 1480-19-9
Price
US $30.00/kg
Min. Order
1kg
Purity
99.9%
Supply Ability
10000
Release date
2023-04-04
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
Hebei Chuanghai Biotechnology Co,.LTD
Product
Fluanisone 1480-19-9
Price
US $19.00/KG
Min. Order
1KG
Purity
99.%
Supply Ability
50 ton
Release date
2024-08-23

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