216-00-2

Basic information

• Product Name: Dibenzo[a,c]naphthacene
• Synonyms: Dibenzo[a,c]naphthacene
• CAS NO: 216-00-2
• Molecular Formula: C26H16
• Molecular Weight: 328.4052
• Mol File: 216-00-2.mol
• Article Data: 4

Chemical Properties

• Melting Point: 265-266 °C(Solv: xylene (1330-20-7))
• Boiling Point: 604.1°Cat760mmHg
• Flash Point: 314.6°C
• Appearance: /
• Density: 1.263g/cm³
• Vapor Pressure: 6.64E-14mmHg at 25°C
• Refractive Index: 1.842
• CAS DataBase Reference: Dibenzo[a,c]naphthacene(CAS DataBase Reference)
• NIST Chemistry Reference: Dibenzo[a,c]naphthacene(216-00-2)
• EPA Substance Registry System: Dibenzo[a,c]naphthacene(216-00-2)

Safety Data

• Hazardous Substances Data: 216-00-2(Hazardous Substances Data)

Usage

InChI:InChI=1/C26H16/c1-2-8-18-14-20-16-26-24-12-6-4-10-22(24)21-9-3-5-11-23(21)25(26)15-19(20)13-17(18)7-1/h1-16H

Upstream product

• 119505-34-9 o-tolyl-triphenylen-2-yl ketone 
• 859745-96-3 dibenzo[a,c]naphthacene-9,16-dione 
• 31540-88-2 (E)-3-(2-Chloro-phenyl)-2-{3-[(E)-2-(2-chloro-phenyl)-1-cyano-vinyl]-naphthalen-2-yl}-acrylonitrile 
• 7651-80-1 1-fluoroanthracene 
• 77037-26-4 1,2,3,4-tetrahydro-1,4-epoxytriphenylene 
• 235-94-9 Phenanthro[9,10-c]furan 
• 77037-23-1 1,4,epoxy-1,4-dihydrotriphenylene 
• 872294-17-2 dibenzo[a,c]naphthacene-10,15-dione 
• 110-86-1 pyridine 
• 64-19-7 acetic acid 
• 118522-15-9 9,16-dihydro-9,16-epoxydibenzonaphthacene 
• 84-11-7 9,10-phenanthrenequinone 
• 39013-98-4 2,3-bis(triphenylphosphonium-methyl)-naphthalene dibromide 

Relevant articles and documents

Segregation of Charge in Ions of Dibenzonaphthacene: Relation of Topology and Electronic Structure. An NMR, ESR, and ENDOR Study

1H- and 13C-chemical shifts of the dianion of dibenzonaphthacene (1) have unambiguously been assigned by 2D-NMR spectroscopy.They indicate a remarkable charge distribution, as most of the negative charge is localized on the 'anthracenic' moiety, whil

Benzannulated Isobenzofurans

A number of arynes, generated by treatment of haloarenes with sodium or potassium amide in tetrahydrofuran, were trapped with furan.The resulting dihydro epoxy arenes were converted into the following annulated isobenzofuran derivatives by using reverse Diels-Alder methodology: naphthofuran, phenanthrofuran, pyrenofuran, pyrenofuran, anthrafuran, phenanthrofuran and phenathrofuran.Bimolecular rate constants for the addition of maleic anhydride to these furans were measured, and were correlated with the Herndon structure count.Addition of arynes to selected members of this furan series yielded adducts which were deoxygenated to afford polycyclic aromatic hydrocarbons.