91281-25-3

Basic information

• Product Name: N-ethyl-1-phenyl-N-prop-2-en-1-ylcyclohexanamine hydrochloride
• CAS NO: 91281-25-3
• Molecular Formula: C₁₇H₂₅N*ClH
• Molecular Weight: 279.848
• Mol File: 91281-25-3.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 338.5°C at 760 mmHg
• Flash Point: 143.7°C
• Vapor Pressure: 9.8E-05mmHg at 25°C
• CAS DataBase Reference: N-ethyl-1-phenyl-N-prop-2-en-1-ylcyclohexanamine hydrochloride(CAS DataBase Reference)
• NIST Chemistry Reference: N-ethyl-1-phenyl-N-prop-2-en-1-ylcyclohexanamine hydrochloride(91281-25-3)
• EPA Substance Registry System: N-ethyl-1-phenyl-N-prop-2-en-1-ylcyclohexanamine hydrochloride(91281-25-3)

Safety Data

• Hazardous Substances Data: 91281-25-3(Hazardous Substances Data)

Upstream product

• 591-51-5 phenyllithium 
• 108-94-1 cyclohexanone 
• 22912-24-9 1-ethylamino-1-cyclohexanecarbonitrile 
• 2201-15-2 Cyclohexamine 
• 106-95-6 allyl bromide 

Relevant articles and documents

N-allyl analogues of phencyclidine: Chemical synthesis and pharmacological properties

Several N-allyl derivatives of 1-phenylcyclohexylamine (PCA) were prepared, and their pharmacology was briefly characterized. The mono- and diallyl derivatives 4-7 had phencyclidine-like activities in mice but were less potent behaviorally than phencyclidine (PCP). None were PCP antagonists. In vitro these compounds were competitive inhibitors of butyrylcholinesterase (BChE) and protected against inhibition by DFP. In addition, these agents displaced tritiated N-methyl-4-piperidyl benzilate from mouse-brain homogenates and inhibited the effects of acetylcholine on isolated guinea pig ileum. None of these in vitro effects correlated with their PCP-like behavioral activity in vivo in mice.