ChemicalBook--->CAS DataBase List--->3867-15-0

3867-15-0

3867-15-0 Structure

3867-15-0 Structure
IdentificationBack Directory
[Name]

1-piperidinocyclohexanecarbonitrile
[CAS]

3867-15-0
[Synonyms]

1-PCC
1-piperidinocyclohexanecarbonitrile
1-Piperidine Cyclohexane Carbonitrile
1-piperidin-1-ylcyclohexane-1-carbonitrile
Cyclohexanecarbonitrile, 1-(1-piperidinyl)-
1-piperidinocyclohexanecarbonitrile 3867-15-0 C12H20N2
1-piperidin-1-ylcyclohexanecarbonitrile(SALTDATA: FREE)
[Molecular Formula]

C12H20N2
[MDL Number]

MFCD00179761
[MOL File]

3867-15-0.mol
[Molecular Weight]

192.3
Chemical PropertiesBack Directory
[Boiling point ]

318.3°C (rough estimate)
[density ]

1.0076 (rough estimate)
[refractive index ]

1.5200 (estimate)
[solubility ]

DMF: 2 mg/mL; DMSO: 3 mg/mL; DMSO:PBS(pH 7.2) (1:4): 0.2 mg/mL; Ethanol: 1 mg/mL
[form ]

A crystalline solid
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[HazardClass ]

IRRITANT
Hazard InformationBack Directory
[Description]

1-Piperidinocyclohexanecarbonitrile (Item No. 20367) is an analytical reference standard categorized as a precursor in the synthesis of PCP (Item Nos. ISO60194 | 14276). 1-Piperidinocyclohexanecarbonitrile has been found as a contaminant in PCP preparations. 1-Piperidinocyclohexanecarbonitrile is regulated as a Schedule II compound in the United States. This product is intended for research and forensic applications.
[Uses]

1-Piperidino-1-cyclohexanecarbonitrile is a precursor to the manufacture of Phencyclidine (P295500) which is an anesthetic and controlled substance. 1-Piperidino-1-cyclohexanecarbonitrile is found have a toxicity that is three times greater than that of Phencyclidine.
[References]

[1] L P LUE. Pyrolytic fate of piperidinocyclohexanecarbonitrile, a contaminant of phencyclidine, during smoking.[J]. Journal of analytical toxicology, 1988, 12 2: 57-61. DOI: 10.1093/jat/12.2.57
[2] A T SHULGIN  D E M L. Illicit synthesis of phencyclidine (PCP) and several of its analogs.[J]. Clinical Toxicology, 1976, 9 4: 553-560. DOI: 10.3109/15563657608988157
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