5660-91-3

Basic information

• Product Name: PHENCYCLONE
• Synonyms: PHENCYCLONE;1,3-diphenyl-2H-cyclopenta[l]phenanthren-2-one;1,3-di(phenyl)cyclopenta[l]phenanthren-2-one
• CAS NO: 5660-91-3
• Molecular Formula: C₂₉H₁₈O
• Molecular Weight: 382.45
• EINECS: 227-112-4
• Mol File: 5660-91-3.mol
• Article Data: 14

Chemical Properties

• Melting Point: 245-249°C
• Boiling Point: 673.6°Cat760mmHg
• Flash Point: 294.9°C
• Appearance: /
• Density: 1.29g/cm³
• Vapor Pressure: 5.26E-18mmHg at 25°C
• Refractive Index: 1.739
• BRN: 2061817
• CAS DataBase Reference: PHENCYCLONE(CAS DataBase Reference)
• NIST Chemistry Reference: PHENCYCLONE(5660-91-3)
• EPA Substance Registry System: PHENCYCLONE(5660-91-3)

Safety Data

• Safety Statements: 22-24/25
• Hazardous Substances Data: 5660-91-3(Hazardous Substances Data)

Usage

General Description

Phencyclone, also known as PCPy, is a dissociative anesthetic drug that belongs to the arylcyclohexylamine class of chemicals. It is chemically related to phencyclidine (PCP) and has similar effects, including hallucinations, delusions, and a sense of detachment from reality. Phencyclone is a potent NMDA receptor antagonist, which means it blocks the transmission of signals between the brain and spinal cord. It is commonly used recreationally for its mind-altering effects, but it is also known to produce negative side effects such as agitation, aggressive behavior, and disorientation. Additionally, phencyclone has a high potential for abuse and can cause serious adverse health effects, including addiction, psychosis, and long-term cognitive impairment. It is illegal in many countries and is classified as a Schedule I controlled substance in the United States.

InChI:InChI=1/C29H18O/c30-29-25(19-11-3-1-4-12-19)27-23-17-9-7-15-21(23)22-16-8-10-18-24(22)28(27)26(29)20-13-5-2-6-14-20/h1-18H

Upstream product

• 859182-64-2 11b-hydroxy-1,3-diphenyl-1,11b-dihydro-cyclopenta[l]phenanthren-2-one 
• 84-11-7 9,10-phenanthrenequinone 
• 102-04-5 1,3-Diphenylpropanone 
• 201230-82-2 carbon monoxide 
• 10403-50-6 2,2'-Bis(phenylethynyl)<1,1'-biphenyl> 
• 98239-58-8 2-(1-Oxo-2,11a-diphenyl-1,11a-dihydro-11-aza-cyclopropa[1,5]cyclopenta[1,2-l]phenanthren-11-yl)-isoindole-1,3-dione 
• 64-17-5 ethanol 

Downstream Products

• 854641-50-2 1,4-diphenyl-triphenylene-2,3-dicarboxylic acid-anhydride 
• 57969-65-0 13-oxo-1,4-diphenyl-1,2,3,4-tetrahydro-1ξ,4ξ-methano-triphenylene-2r,3c-dicarboxylic acid-anhydride 
• 854406-35-2 2-hydroxy-2-methyl-1.3-diphenyl-2H-cyclopenta[l]phenanthrene 
• 41442-14-2 1,2,3-triphenylcyclopenta[l]phenanthren-2-ol 
• 38458-30-9 9,10-phenanthrenediylbis(phenylmethanone) 
• 58077-44-4 1,3-dihydro-1,3-diphenylcyclopenta[l]phenanthren-2-one 
• 38458-26-3 1,3-diphenylphenanthro[9,10-c]thiophene 
• 6243-69-2 1,2,3-triphenyl-2H-dibenz[e,g]isoindole 
• 55082-19-4 1,2,4-triphenyltriphenylene 
• 36262-81-4 1,2,3,4-tetraphenyltriphenylene 

Relevant articles and documents

1,4-Diphenyltriphenylene grafted polysiloxane as a stationary phase for gas chromatography

In this work, 1,4-diphenyltriphenylene-grafted (14.2%) polysiloxane (DPTP) was successfully synthesized and statically coated on capillary columns as a stationary phase for gas chromatography. The DPTP columns exhibited excellent efficiencies of 3646 plates m-1 for a 30 m column and 3125 plates m-1 for a 10 m column, as evidenced by naphthalene measurements at 120 °C, which demonstrated the good film-forming ability of DPTP. Thermogravimetric analysis showed that the weight of DPTP is reduced by 2% at 380 °C. Separation of the polyethylene pyrolysis product indicated that the maximum allowable operating temperature of the DPTP column is 360 °C. The moderate polarity of the DPTP column was investigated in terms of McReynolds constants. The DPTP column was utilized to separate analytes, including aromatic isomers, fatty acid esters, ethers, polycyclic aromatic hydrocarbons and their derivatives, and nitrogenous heterocyclic compounds, on the basis of the column's strong π-π stacking, dipole-induced dipole, and dispersion interactions with solutes. In general, the DPTP column offers great potential as a novel stationary phase for separating various analytes due to its special structure and remarkable separation performance.

Controlled deposition of large-area and highly-ordered thin films: effect of dip-coating-induced morphological evolution on resistive memory performance

Developing a simple, versatile and efficient technique that enables both large-scale production and nano-scale control is highly desirable but very challenging for achieving high-performance organic-based memory electronic devices. Herein, we employed a dip-coating method to fabricate reliable and cost-effective organic memory devices (OMDs). This technique enables us to deposit high-quality, homogeneous and large-area nanopatterns on the surfaces of thin films and realize uniform OMD performances with a record reproducibility up to 96%. To the best of our knowledge, this is the first report on dip-coated OMDs with the highest reproducibility observed to date, which demonstrates the promising versatility of the dip-coating technique to fabricate organic memory devices and its suitability to scale-up for high-throughput solution processing.

NITROGEN-CONTAINING POLYCYCLIC COMPOUND

To provide a nitrogen-containing polycyclic compound that can be suitably used as an oxygen reduction catalyst.SOLUTION: A nitrogen-containing polycyclic compound is illustrated by the formula (5), where n is the number of 1 or more, normally 1000 or less.SELECTED DRAWING: None