207-18-1

Basic information

• Product Name: NAPHTHO[2,3-K]FLUORANTHENE
• Synonyms: NAPHTHO[2,3-K]FLUORANTHENE;Acenaphth(1,2-B)anthracene
• CAS NO: 207-18-1
• Molecular Formula: C24H14
• Molecular Weight: 302.37
• Mol File: 207-18-1.mol
• Article Data: 4

Chemical Properties

• Melting Point: 301-302 °C
• Boiling Point: 552.3°Cat760mmHg
• Flash Point: 282°C
• Appearance: /
• Density: 1.313g/cm³
• Vapor Pressure: 1.12E-11mmHg at 25°C
• Refractive Index: 1.912
• CAS DataBase Reference: NAPHTHO[2,3-K]FLUORANTHENE(CAS DataBase Reference)
• NIST Chemistry Reference: NAPHTHO[2,3-K]FLUORANTHENE(207-18-1)
• EPA Substance Registry System: NAPHTHO[2,3-K]FLUORANTHENE(207-18-1)

Safety Data

• Hazardous Substances Data: 207-18-1(Hazardous Substances Data)

Usage

Uses

Acenaphth[1,2-b]anthracene is mutagenic. It is a ubiquitous pollutant in urban air that may pose risks to human health. It is also used as a standard in determination of polycyclic aromatic hydrocarbons (PAH’s).

InChI:InChI=1/C24H14/c1-2-6-17-12-19-14-23-21-10-4-8-15-7-3-9-20(24(15)21)22(23)13-18(19)11-16(17)5-1/h1-14H

Upstream product

• 76727-40-7 6b,7-dihydronaphtho<2,3-k>fluoranthene 
• 39013-98-4 2,3-bis(triphenylphosphonium-methyl)-naphthalene dibromide 
• 82-86-0 acenaphthene quinone 
• 92012-57-2 1-(diphenylmethylidene)-1H-cyclopropa[b]naphthalene 
• 109685-01-0 fluorenylidenecyclopropa[b]naphthalene 
• 769958-81-8 naphtho[2,3-k]fluoranthene-8,13-dione 
• 581-40-8 2,3-dimethylnaphthalene 
• 38998-33-3 2,3-di(bromomethyl)naphthalene 

Relevant articles and documents

Modular Design of Fluorescent Dibenzo- and Naphtho-Fluoranthenes: Structural Rearrangements and Electronic Properties

A library of 12 dibenzo- and naphtho-fluoranthene polycyclic aromatic hydrocarbons (PAHs) with MW = 302 (C24H14) was synthesized via a Pd-catalyzed fluoranthene ring-closing reaction. By understanding the various modes by which the palladium migrates during the transformation, structural rearrangements were bypassed, obtaining pure PAHs in high yields. Spectroscopic and electrochemical characterization demonstrated the profound diversity in the electronic structures between isomers. Highlighting the significant differences in emission of visible light, this library of PAHs will enable their standardization for toxicological assessment and potential use as optoelectronic materials.

A Facile Synthesis of Some Polycyclic Hydrocarbons: Application of Phase Transfer Catalysis in the Bis-Wittig Reaction

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