Identification | Back Directory | [Name]
OPIPRAMOL DIHYDROCHLORIDE | [CAS]
909-39-7 | [Synonyms]
ensidon insidondihydrochloride opipramolhydrochloride Opipramol dihydrochloride >=98% (HPLC), solid 4-(3-(5h-dibenz(b,f)azepin-5-yl)propyl)-1-piperazineethanodihydrochloride 4-[3-(5H-dibenz(b,f)azepin-5-yl)propyl]piperazine-1-ethanol dihydrochloride 4-(3-(5h-dibenzo(b,f)azepina-5-il)propil)-1-(2-idrossietil)piperazinadiclori 5-(gamma-(beta-hydroxyethylpiperazino)propyl)-5h-dibenzo(b,f)azepinedihydroc Opipramol DihydrochlorideQ: What is
Opipramol Dihydrochloride Q: What is the CAS Number of
Opipramol Dihydrochloride Q: What is the storage condition of
Opipramol Dihydrochloride | [EINECS(EC#)]
213-000-2 | [Molecular Formula]
C23H31Cl2N3O | [MDL Number]
MFCD00941483 | [MOL File]
909-39-7.mol | [Molecular Weight]
436.418 |
Hazard Information | Back Directory | [Originator]
Insidon,Geigy,W. Germany,1962 | [Uses]
antidepressant, antipsychotic;'sigma antagonist | [Manufacturing Process]
A solution of 5-(3-toluene-p-sulfonyloxypropyl)dibenzazepine (9.2g) and 1-(2hydroxyethyl)piperazine (8.6g) in anhydrous toluene (50 cc) is heated at boiling point under reflux for 4 hours.
After cooling, distilled water (75 cc) is added. The aqueous phase is decanted. The toluene solution is washed with distilled water (25 cc) and then extracted with N hydrohloric acid (40 cc). The hydrochloric acid solution is made alkaline to phenolphthalein with sodium hydroxide (d = 1.33).The base which separates is extracted with chloroform (50 cc). The chloroform solution is dried over anhydrous sodium sulfate and then evaporated to dryness. There are obtained 5-[3-(4-β-hydroxyethylpiperazino)propyl]dibenzazepine (7.95g), the dihydrochloride of which, crystallized from ethanol, melts at about 210°C. | [Therapeutic Function]
Antidepressant, Antipsychotic |
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