cas 2201-15-2, Eticyclidine | Articles data ｜lookchem

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2201-15-2

Articles about 2201-15-2Total 5 be found

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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.
Kalir,Teomy,Amir,Fuchs,Lee,Holsztynska,Rocki,Domino
p. 1267 - 1271
(2007/10/02)

Carbon-13 nuclear magnetic resonance spectra of phenycyclidine analogs
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Brine,Williams,Boldt,Carroll
p. 1425 - 1429
(2007/10/05)

Identification of a street drug as N-ethyl-1-phenylcyclohexylamine, a phencyclidine analog
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Bailey
p. 885 - 886
(2007/10/06)

1-Phenycycloalkylamine derivatives. II. Synthesis and pharmacological activity.
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Kalir,Edery,Pelah,Balderman,Porath
p. 473 - 477
(2007/10/05)

THE SYNTHESIS OF PHENCYCLIDINE AND OTHER 1-ARYLCYCLOHEXYLAMINES.
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MADDOX,GODEFROI,PARCELL
p. 230 - 235
(2007/10/04)

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91281-25-3
N-allyl-N-ethyl-1-phenylcyclohexylamine hydrochloride

Chemical Properties

Melting Point: 102.5-103.5 °C
Boiling Point: 301.1 °C at 760 mmHg
Flash Point:136.8 °C
Density: 0.96 g/cm³
Vapor Pressure: 0.00108mmHg at 25°C
Refractive Index: 1.532
PKA: 10.17±0.20(Predicted)
PSA: 12.03000
LogP: 3.84640

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