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CAS

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79787-43-2

3-Hydroxyphencyclidine (3-HO-PCP) is a dissociative hallucinogen belonging to the arylcyclohexylamine class, closely related to phencyclidine (PCP). It has been marketed as a designer drug and has gained attention due to its potential misuse and associated risks.
Used in Research and Forensic Analysis:
3-Hydroxyphencyclidine is used as a research chemical for studying the effects and mechanisms of action of dissociative hallucinogens. It aids in understanding the structure-activity relationships and potential therapeutic applications of these compounds.
Used in Drug Policy and Regulation:
3-Hydroxyphencyclidine is used as a reference point in drug policy and regulation discussions, particularly in the context of the Misuse of Drugs Act (1971) in the United Kingdom. The Advisory Council on the Misuse of Drugs has suggested that 3-HO-PCP and other arylcyclohexamines should be classified as Class B drugs, highlighting the need for a catch-all clause to cover both existing and unresearched compounds in this class.

79787-43-2 Suppliers

This product is a nationally controlled contraband or patented product, and the Lookchem platform doesn't provide relevant sales information.
  • 79787-43-2 Structure

  • Basic information

    1. Product Name: 3-hydroxyphencyclidine
    2. Synonyms: 3-hydroxyphencyclidine;3HOPCP;3-ho-pcp
    3. CAS NO:79787-43-2
    4. Molecular Formula: C17H25NO
    5. Molecular Weight: 259.3865
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 79787-43-2.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 393.7°C at 760 mmHg
    3. Flash Point: 185.6°C
    4. Appearance: /
    5. Density: 1.086g/cm3
    6. Vapor Pressure: 9.17E-07mmHg at 25°C
    7. Refractive Index: 1.572
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 3-hydroxyphencyclidine(CAS DataBase Reference)
    11. NIST Chemistry Reference: 3-hydroxyphencyclidine(79787-43-2)
    12. EPA Substance Registry System: 3-hydroxyphencyclidine(79787-43-2)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 79787-43-2(Hazardous Substances Data)

79787-43-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79787-43-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,7,8 and 7 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 79787-43:
(7*7)+(6*9)+(5*7)+(4*8)+(3*7)+(2*4)+(1*3)=202
202 % 10 = 2
So 79787-43-2 is a valid CAS Registry Number.
InChI:InChI=1/C17H25NO/c19-16-9-7-8-15(14-16)17(10-3-1-4-11-17)18-12-5-2-6-13-18/h7-9,14,19H,1-6,10-13H2

79787-43-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(1-piperidin-1-ylcyclohexyl)phenol

1.2 Other means of identification

Product number -
Other names 3-(PIPERIDIN-1-YLCYCLOHEXYL)PHENOL

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:79787-43-2 SDS

79787-43-2Relevant articles and documents

Novel analogues of ketamine and phencyclidine as NMDA receptor antagonists

Zarantonello, Paola,Bettini, Ezio,Paio, Alfredo,Simoncelli, Chiara,Terreni, Silvia,Cardullo, Francesco

, p. 2059 - 2063 (2011/04/24)

The identification of structurally novel analogues of ketamine and phencyclidine (PCP), as NMDA receptor antagonists, with low to moderate potency at GluN2A and GluN2B receptors is discussed. In particular, some examples, such as compounds 6 and 10, shows decreased calculated lipophilicity, when compared to PCP, while retaining moderate activity. Moreover, the germinal aryl amino substituted lactam ring, as exemplified in compounds 7-10 and 11-13, constitutes a novel scaffold with potential application in the design of biologically active compounds.

Synthesis and brain distribution of carbon-11 labeled analogs of antagonists for the NMDA receptor coupled PCP-binding site

Haradahira, Terushi,Sasaki, Sigeki,Maeda, Minoru,Kobayashi, Kaoru,Inoue, Osamu,Tomita, Urara,Nishikawa, Toru,Suzuki, Kazutoshi

, p. 843 - 858 (2007/10/03)

Two phencyclidine (PCP) analogs, 3 and 4, and one thienylcyclohexylpiperidine (TCP) analog, (±)6, were labeled with positron emitter carbon-11. These compounds displayed higher in vitro binding affinities than PCP itself for the PCP-binding site located inside the ion channel on the N-methyl-D-aspartate (NMDA) receptors. Brain distribution studies in mice showed different uptake characteristics between the PCP and TCP analogs, indicating their different in vivo interactions with the brain components including the PCP-binding site probably due to the different physicochemical properties of the molecules.