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Conditions | Yield |
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With acetic acid; platinum Hydrogenation; | |
With acetic acid; platinum Hydrogenation; |
Conditions | Yield |
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Multi-step reaction with 2 steps 1: diethyl ether 2: platinum; aqueous acetic acid / Hydrogenation View Scheme |
procyclidine
Conditions | Yield |
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Multi-step reaction with 2 steps 1: diethyl ether 2: platinum; aqueous acetic acid / Hydrogenation View Scheme |
Conditions | Yield |
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With benzene |
ethyl iodide
procyclidine
(+/-)-1-ethyl-1-(3-cyclohexyl-3-hydroxy-3-phenyl-propyl)-pyrrolidinium; iodide
Conditions | Yield |
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With ethanol |
procyclidine
methyl iodide
(+/-)-1-(3-cyclohexyl-3-hydroxy-3-phenyl-propyl)-1-methyl-pyrrolidinium; iodide
Conditions | Yield |
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With acetone |
procyclidine
(S)-Procyclidine
procyclidine
(R)-Procyclidine
procyclidine
(S)-Tricylamol iodide
Conditions | Yield |
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Multi-step reaction with 2 steps 2: acetone / 3 h / Ambient temperature View Scheme |
Chemical Name: Procyclidine
IUPAC NAME: 1-Cyclohexyl-1-phenyl-3-pyrrolidin-1-ylpropan-1-ol
CAS No.: 77-37-2
EINECS: 201-023-0
Molecular Formula: C19H29NO
Molecular Weight: 287.44 g/mol
Density: 1.057 g/cm3
Flash Point: 205.7 °C
Boiling Point: 433.5 °C at 760 mmHg
Following is the structure of 1-Cyclohexyl-1-phenyl-3-pyrrolidino-1-propanol (CAS No.77-37-2):
The chemical synonymous of 1-Cyclohexyl-1-phenyl-3-pyrrolidino-1-propanol (CAS No.77-37-2) are 1-Cyclohexyl-1-Phenyl-3-Pyrrolidin-1-Ylpropan-1-Ol ; Procyclidine ; Tricyclamol ; Kemadrine ; Vagosin ; Α-Cyclohexyl-Α-Phenyl-1-Pyrrolidine-1-Propanol
1. | ipr-mus LD50:131 mg/kg | 27ZQAG Psychotropic Drugs and Related Compounds E. Usdin andD.H. Efron,2nd ed.,Washington, DC.: 1972,291. | ||
2. | ivn-mus LD50:60 mg/kg | 27ZQAG Psychotropic Drugs and Related Compounds E. Usdin andD.H. Efron,2nd ed.,Washington, DC.: 1972,291. |
A poison by intraperitoneal and intravenous routes. When heated to decomposition it emits toxic fumes of NOx.