Melperone Hydrochloride

CAS: 1622-79-3

Ref. TR-M216800

Produktinformation

• Name: Melperone Hydrochloride
• Synonyme: 1-(4-Fluorophenyl)-4-(4-methyl-1-piperidinyl)-1-butanone, Methylperone Hydrochloride, Flubuperone Hydrochloride, 4-Fluoro-?-(4-methylpiperidino)butyrophenone Hydrochloride, 4'-Fluoro-4-(4-methylpiperidino)butyrophenone Hydrochloride, Buronil Hydrochloride, FG 5111 Hydrochloride, ?-(4-Methylpiperidino)-p-fluorobutyrophenone Hydrochloride, 1-(4-Fluorophenyl)-4-(4-Methylpiperazin-1-Yl)Butan-1-One Hydrochloride, 1-(4-Fluorophenyl)-4-(4-Methylpiperidin-1-Yl)Butan-1-One, 1-(4-Fluorophenyl)-4-(4-methylpiperidin-1-yl)butan-1-one hydrochloride, 1-Butanone, 1-(4-fluorophenyl)-4-(4-methyl-1-piperidinyl)-, hydrochloride, 1-Butanone, 1-(4-fluorophenyl)-4-(4-methyl-1-piperidinyl)-, hydrochloride (1:1), 1-[4-(4-Fluorophenyl)-4-Oxobutyl]-4-Methylpiperidinium Chloride, 4'-Fluoro-4-(4-methylpiperidino)butyrophenone hydrochloride, Buronil, Butyrophenone, 4'-fluoro-4-(4-methylpiperidino)-, hydrochloride, Eunerpan, Fg 5111, Melpax, Melperone HCl, Melperone hydrochloride, Methylperone chloride, Methylperone hydrochloride, Unii-88G640374K, gamma-(4-Methylpiperidine)-p-fluorobutyrophenone hydrochloride, 1-(3-(p-Fluorobenzoyl)propyl)-4-methylpiperazinium chloride

Beschreibung

Applications Melperone is a neuroleptic butyrophenone. Melperone is also an antiarrhythmic agent. Melperone is an effective atypical antipsychotic drug used in the treatment of schizophrenia.
References Petersen, E.N. et al.: Acta Pharmacol. Toxicol., 42, 388 (1978); Platou, E. et al.: Acta Pharmacol. Toxicol., 50, 108 (1982); Bjerkenstedt, L. et al.: Acta Psych. Scand. Supp., 352, 35 (1989); Meltzer, H.Y. et al.: Psych. Res., 105, 201 (2001);

• Marke: TRC

Chemische Eigenschaften

• Molekulargewicht: 299.81
• Formel: C₁₆H₂₂FNO·ClH
• Farbe/Form: White To Brown
• InChl: InChI=1S/C16H22FNO.ClH/c1-13-8-11-18(12-9-13)10-2-3-16(19)14-4-6-15(17)7-5-14;/h4-7,13H,2-3,8-12H2,1H3;1H
• InChI Key: InChIKey=MQHYXXIJLKFQGY-UHFFFAOYSA-N
• SMILES: CC1CCN(CCCC(=O)c2ccc(F)cc2)CC1.Cl