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Eticyclidine, also known as Etic or Benzo, is a dissociative anesthetic and a derivative of cyclohexamine. It was first synthesized in the 1950s and has been used in veterinary medicine for its sedative and analgesic properties. Structurally, it is similar to ketamine and phencyclidine (PCP), and it shares their dissociative effects, which involve a detachment from one's own body and surroundings. Eticyclidine is known for its potential to cause hallucinations, out-of-body experiences, and a sense of euphoria. However, it is not approved for human use due to its psychoactive effects and potential for abuse. It is important to note that the use of eticyclidine is illegal in many countries and can pose serious health risks, including addiction and severe psychological effects.

2201-15-2

2201-15-2 Suppliers

This product is a nationally controlled contraband or patented product, and the Lookchem platform doesn't provide relevant sales information.

2201-15-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2201-15-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,0 and 1 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2201-15:
(6*2)+(5*2)+(4*0)+(3*1)+(2*1)+(1*5)=32
32 % 10 = 2
So 2201-15-2 is a valid CAS Registry Number.
InChI:InChI=1/C14H21N/c1-2-15-14(11-7-4-8-12-14)13-9-5-3-6-10-13/h3,5-6,9-10,15H,2,4,7-8,11-12H2,1H3

2201-15-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-ethyl-1-phenylcyclohexan-1-amine

1.2 Other means of identification

Product number -
Other names Eticyclidinum [INN-Latin]

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:2201-15-2 SDS

2201-15-2Relevant academic research and scientific papers

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

Kalir,Teomy,Amir,Fuchs,Lee,Holsztynska,Rocki,Domino

, p. 1267 - 1271 (2007/10/02)

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.