4325-76-2

Basic information

• Product Name: 1-phenylphenanthrene
• Synonyms: 1-phenylphenanthrene
• CAS NO: 4325-76-2
• Molecular Formula: C₂₀H₁₄
• Molecular Weight: 254.32516
• Mol File: 4325-76-2.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 431.3°Cat760mmHg
• Flash Point: 207.8°C
• Appearance: /
• Density: 1.14g/cm³
• Vapor Pressure: 3.05E-07mmHg at 25°C
• Refractive Index: 1.703
• CAS DataBase Reference: 1-phenylphenanthrene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-phenylphenanthrene(4325-76-2)
• EPA Substance Registry System: 1-phenylphenanthrene(4325-76-2)

Safety Data

• Hazardous Substances Data: 4325-76-2(Hazardous Substances Data)

Usage

Polycyclic aromatic hydrocarbon

1-Phenylphenanthrene is a type of hydrocarbon that consists of multiple aromatic rings.

Composition

It is composed of a phenanthrene ring with a phenyl group attached at the 1-position.

Physical properties

1-Phenylphenanthrene is a colorless, crystalline solid that is insoluble in water but soluble in organic solvents.

Uses

It is commonly used as a building block in the synthesis of various pharmaceutical and organic compounds.

Potential applications

1-Phenylphenanthrene has potential applications in organic light-emitting diodes (OLEDs) and organic photovoltaic devices.

Research interest

Due to its chemical structure and properties, 1-phenylphenanthrene is of interest in the field of materials science and organic chemistry research.

InChI:InChI=1/C20H14/c1-2-7-15(8-3-1)18-11-6-12-19-17-10-5-4-9-16(17)13-14-20(18)19/h1-14H

Upstream product

• 110248-30-1 1-cyclohexyl-phenanthrene 
• 113135-70-9 (+/-)-1-Hydroxy-1-phenyl-1.2.3.4-tetrahydro-phenanthren 
• 95813-89-1 1-phenyl-1,9,10,10a-tetrahydro-2H-phenanthren-3-one 
• 2113-51-1 2-iodobiphenyl 
• 121-46-0 bicyclo[2.2.1]hepta-2,5-diene 
• 7154-66-7 2-bromobenzoic acid chloride 
• 88-65-3 2-bromobenzoic-acid 
• 2052-07-5 2-Bromobiphenyl 
• 536-74-3 phenylacetylene 
• 591-50-4 iodobenzene 
• 573-57-9 1,4-dihydronaphthalene-1,4-epoxide 
• 781-74-8 4-(1-naphthyl)butanoic acid 
• 85-01-8 phenanthrene 
• 542-18-7 cyclohexyl chloride 

Downstream Products

• 122094-95-5 1-phenyl-dibenzo[a,c]phenazine 
• 117000-39-2 8-phenyl-benz[de]anthracen-7-one 
• 112553-93-2 1-phenyl-phenanthrene-9,10-dione 

Relevant articles and documents

A novel and efficient synthesis of phenanthrene derivatives via palladium/norbornadiene-catalyzed domino one-pot reaction

Herein we report a novel palladium-catalyzed reaction that results in phenanthrene derivatives using aryl iodides, ortho-bromoben-zoyl chlorides and norbornadiene in one pot. This dramatic transformation undergoes ortho-C–H activation, decarbonylation and subsequent a retro-Diels–Alder process. Pleasantly, this protocol has a wider substrate range, shorter reaction times and higher yields of products than previously reported methods.

[4 + 2] Annulation of Donor-Acceptor Cyclopropanes with Acetylenes Using 1,2-Zwitterionic Reactivity

A new process for the [4 + 2] annulation of donor-acceptor cyclopropanes with acetylenes under the effect of anhydrous GaCl3 using 1,2-zwitterion reactivity was elaborated. The reaction opens access to substituted dihydronaphthalenes, naphthalenes, and other fused carbocycles. The direction of the reaction can be efficiently controlled by temperature.

A convergent approach to polycyclic aromatic hydrocarbons

A new concise route to Polycyclic Aromatic Hydrocarbons (PAHs) through radical addition and cyclisation of xanthates is described. The Royal Society of Chemistry 2011.