60756-83-4

Basic information

• Product Name: 4-phenyl-4-piperidinocyclohexanol
• Synonyms: 4-phenyl-4-piperidinocyclohexanol
• CAS NO: 60756-83-4
• Molecular Formula: C₁₇H₂₅NO
• Molecular Weight: 259.39
• Mol File: 60756-83-4.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 382.5°C at 760 mmHg
• Flash Point: 83.4°C
• Appearance: /
• Density: 1.093g/cm³
• Vapor Pressure: 1.56E-06mmHg at 25°C
• Refractive Index: 1.574
• CAS DataBase Reference: 4-phenyl-4-piperidinocyclohexanol(CAS DataBase Reference)
• NIST Chemistry Reference: 4-phenyl-4-piperidinocyclohexanol(60756-83-4)
• EPA Substance Registry System: 4-phenyl-4-piperidinocyclohexanol(60756-83-4)

Safety Data

• Hazardous Substances Data: 60756-83-4(Hazardous Substances Data)

Usage

InChI:InChI=1/C17H25NO/c19-16-9-11-17(12-10-16,15-7-3-1-4-8-15)18-13-5-2-6-14-18/h1,3-4,7-8,16,19H,2,5-6,9-14H2

Upstream product

• 77-10-1 Phencyclidine 
• 23510-95-4 4-benzoyloxycyclohexanone 
• 6091-44-7 piperidine hydrochloride 
• 60-29-7 diethyl ether 
• 100-58-3 phenylmagnesium bromide 

Downstream Products

• 110915-02-1 1-phenyl-1-piperidino-4-methylenecyclohexane 
• 55040-03-4 cis-Ph/Me 1-(1-phenyl-4-methylcyclohexyl)piperidine 
• 29084-52-4 trans-Ph/Me 1-(1-phenyl-4-methylcyclohexyl)piperidine 
• 65620-13-5 4-phenyl-4-(1-piperidinyl)cyclohexanone 
• 120807-75-2 1-(1-Phenyl-4-trimethylsilanyloxy-cyclohexyl)-piperidine 

Relevant articles and documents

Phencyclidine compounds and assays for its determination

Novel derivatives of phencyclidine are provided as precursors for conjugating to antigenic proteins for the preparation of antibodies which bind to phencyclidine or conjugation to enzymes for use as reagents in immunoassays. The combination of the antibodies and enzyme conjugates provide a sensitive and rapid assay for phencyclidine.

AN EFFICIENT SYNTHESIS OF 1-PHENYL-1-PIPERIDINO-trans-4-METHYLCYCLOHEXANE: UNANTICIPATED TOTAL STEREOSELECTIVITY IN THE CATALYTIC HYDROGENATION OF AN OLEFIN

A superior synthesis of the title compound, 1-phenyl-1-piperidino-trans-4-methylcyclohexane, is reported.The key step, the catalytic hydrogenation of 1-phenyl-1-piperidino-4-methylenecyclohexane hydrochloride, proceeds with unusual stereospecificity via a