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Amperozide

Product Name
Amperozide
CAS No.
75558-90-6
Chemical Name
Amperozide
Synonyms
FG-5606;Amperozide;Amperozida;Amperozidum;4-[4,4-bis(4-fluorophenyl)butyl]-N-ethylpiperazine-1-carboxamide;4-[4,4-Bis(4-fluorophenyl)butyl]-N-ethyl-1-piperazinecarboxamide;1-Piperazinecarboxamide, 4-[4,4-bis(4-fluorophenyl)butyl]-N-ethyl-
CBNumber
CB71178020
Molecular Formula
C23H29F2N3O
Formula Weight
401.498
MOL File
75558-90-6.mol
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Amperozide Property

Boiling point:
579.5±50.0 °C(Predicted)
Density 
1.151±0.06 g/cm3(Predicted)
storage temp. 
Store at +4°C
pka
14.59±0.20(Predicted)
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

American Custom Chemicals Corporation
Product number
API0008640
Product name
AMPEROZIDE
Purity
95.00%
Packaging
10MG
Price
$665.81
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
API0008640
Product name
AMPEROZIDE
Purity
95.00%
Packaging
50MG
Price
$1073.29
Updated
2021/12/16
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Amperozide Chemical Properties,Usage,Production

Originator

Amperozide,Ferrosan

Manufacturing Process

(1). A stirred mixture of 4.7 g (0.03 mole) of N'-ethyl-1- piperazinecarboxamide, 10.1 g (0.036 mole) of 4-chloro-1,1-(di-pfluorophenyl) butane, 5.0 g of sodium bicarbonate and 10 ml of ethanol was heated at reflux for 60 hours. 50 ml of water was added. The mixture was extracted twice with ether. The combined extracts were dried over sodium sulfate and concentrated. The residue was dissolved in ethanol-ether and the hydrochloride was precipitated with hydrogen chloride in ethanol. The solid was collected by filtration and recrystallised from 2-butanone-isopropanol 4:1 to give 6.4 g of N'-ethyl-4-[4,4-(di-p-fluorophenyl)butyl]-1- piperazinecarboxamide hydrochloride. Melting point 177-178°C.
(2). A stirred mixture of 9.9 g (0.03 mole) of 1-[4,4-(di-pfluorophenyl) butyl]piperazine, 5,0 g (0,03 mole) of phenyl N-ethylcarbamate, 6,6 g of potassium carbonate and 100 ml of toluene was heated at reflux for 45 minutes. The mixture was filtered and the solvent was removed. The residual oil was dissolved in ethanol-ether and the hydrochloride was precipitated with hydrogen chloride in ethanol. The solid was collected by filtration and recrystallized from 2-butanone-isopropanol 4:1 to give 6.8 g of N'-ethyl-4-[4,4-(di-p-fluorophenyl)butyl]-1-piperazinecarboxamide hydrochloride. Melting point 177-178°C.

Therapeutic Function

Anti-aggressive, Antiarrhythmic

Biological Activity

Atypical antipsychotic that displays high affinity for 5-HT 2 receptors (K i = 26 nM) and low affinity for D 2 receptors. Supresses ethanol drinking in genetically ethanol-preferring rats.

Amperozide Preparation Products And Raw materials

Raw materials

Preparation Products

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Amperozide Suppliers

EMMX Biotechnology LLC
Tel
888-539-0666
Fax
888-539-0666
Email
info@emmx.com
Country
United States
ProdList
8449
Advantage
60
TargetMol Chemicals Inc.
Tel
+1-781-999-5354 +1-00000000000
Email
marketing@targetmol.com
Country
United States
ProdList
19892
Advantage
58

75558-90-6, AmperozideRelated Search:


  • Amperozide
  • 4-[4,4-Bis(4-fluorophenyl)butyl]-N-ethyl-1-piperazinecarboxamide
  • FG-5606
  • 4-[4,4-bis(4-fluorophenyl)butyl]-N-ethylpiperazine-1-carboxamide
  • 1-Piperazinecarboxamide, 4-[4,4-bis(4-fluorophenyl)butyl]-N-ethyl-
  • Amperozida
  • Amperozidum
  • 75558-90-6
  • C23H29F2N3OHCl
  • C23H29F2N3O
  • Serotonin receptor