ChemicalBook--->CAS DataBase List--->5966-41-6

5966-41-6

5966-41-6 Structure

5966-41-6 Structure
IdentificationBack Directory
[Name]

diisopromine
[CAS]

5966-41-6
[Synonyms]

R 253
Do-Bil
Hepabyl
Hepacol
Megabyl
Cholagol
DisproMine
Disopromine
diisopromine
N,N-Diisopropyl-3,3- diphenylpropylaMine
N,N-Diisopropyl-3,3-diphenyl-1-propanamine
3,3-diphenyl-N,N-di(propan-2-yl)propan-1-amine
N,N-Bis(1-Methylethyl)-γ-phenylbenzenepropanaMine
Benzenepropanamine, N,N-bis(1-methylethyl)-γ-phenyl-
[EINECS(EC#)]

227-752-4
[Molecular Formula]

C21H29N
[MDL Number]

MFCD00865196
[MOL File]

5966-41-6.mol
[Molecular Weight]

295.46
Hazard InformationBack Directory
[Originator]

Agofell,Janssen-Cilag
[Uses]

Spasmolitic; choleretic.
[Definition]

ChEBI: Diisopromine is a diarylmethane.
[Manufacturing Process]

A vigorously stirred suspension of 0.2 to 1 mole of sodium amide in 200 ml of xylene, in which 0.1 moles of 4-diisopropylamino-2,2-diphenyl-butyronitrile were dissolved, was boiled for about twelve hours. After this the excess of sodium amide was decomposed with water and the xylene layer was separated, washed with water and extracted with dilute hydrochloric acid. This acidic extract was made strongly alkaline with a concentrated aqueous sodium hydroxide solution and the separated base was extracted with ether. After drying, the ether evaporated and the 1,1-diphenyl-3-diisopropylaminopropane was distilled in vacuum. The oil obtained can be dissolved in ether and after introduction of hydrochloric acid gas the hydrochloric acid addition salt precipitates. It shows a melting point of 171°C.
[Therapeutic Function]

Spasmolytic, Choleretic
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