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ChemicalBook--->CAS DataBase List--->3575-80-2

3575-80-2

3575-80-2 Structure

3575-80-2 Structure
IdentificationBack Directory
[Name]

MELPERONE
[CAS]

3575-80-2
[Synonyms]

Buronil
FG 5111
Melperon
metylperon
Flubuperone
Melperone >
Melperone,Inhibitor,inhibit
Melperone (base and/or unspecified salts)
γ-(4-Methylpiperidino)-p-fluorobutyrophenone
4-Fluoro-γ-(4-Methylpiperidino)butyrophenone
4'-Fluoro-4-(4-Methylpiperidino)butyrophenone
1-(4-Fluorophenyl)-4-(4-methylpiperidin-1-yl)-1-butanone
1-(4-Fluorophenyl)-4-(4-methylpiperidin-1-yl)butan-1-one
1-(4-Fluorophenyl)-4-(4-Methyl-1-piperidinyl)-1-butanone
1-Butanone, 1-(4-fluorophenyl)-4-(4-methyl-1-piperidinyl)-
[EINECS(EC#)]

609-173-2
[Molecular Formula]

C16H22FNO
[MDL Number]

MFCD00867737
[MOL File]

3575-80-2.mol
[Molecular Weight]

263.354
Chemical PropertiesBack Directory
[Melting point ]

78.0 to 82.0 °C
[Boiling point ]

bp0.1 120-125°
[density ]

1.046±0.06 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

DMSO: 41.67 mg/mL (158.23 mM)
[form ]

powder to crystal
[pka]

9.34±0.10(Predicted)
[color ]

White to Light yellow to Light orange
[Merck ]

14,5827
Safety DataBack Directory
[HS Code ]

2933.39.3100
Hazard InformationBack Directory
[Originator]

Eunerpan,Nordmark,W. Germany,1965
[Definition]

ChEBI: 1-(4-fluorophenyl)-4-(4-methyl-1-piperidinyl)-1-butanone is an aromatic ketone.
[Manufacturing Process]

A solution or dispersion consisting of 20.1 g (0.1 mol) of γ-chloro-pfluorobutyrophenone, 19.8 g (0.2 mol) of 4-methylpiperidine and 0.1 g of potassium iodide in 150 ml toluene is heated in a sealed glass tube for 15 hours at 100°C to 110°C. The potassium iodide and the 4-methylpiperidine hydrochloride formed in the reaction are separated by filtration and the solvent removed from the filtrate by evaporation in vacuum on a steam bath. The residue is distilled and the fraction obtained at 120°C to 125°C and at a pressure lower than 0.1 mm Hg is collected. The base is dissolved in ether and the 4-fluoro-γ-(4-methylpiperidino)-butyrophenone precipitated as the hydrochloride. The reaction product is purified by recrystallization in ethanol/ether.
Yield 22.0 g (73% of theory). MP 209°C to 211°C.
[Therapeutic Function]

Neuroleptic
Spectrum DetailBack Directory
[Spectrum Detail]

MELPERONE(3575-80-2)1HNMR
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