Coronene
Title: Coronene
CAS Registry Number: 191-07-1
Molecular Formula: C24H12
Molecular Weight: 300.35
Percent Composition: C 95.97%, H 4.03%
Literature References: Planar polycyclic aromatic hydrocarbon; found in almost pure form as the mineral pendletonite. Environmental pollutant produced as a byproduct of hydrocarbon combustion; impurity in natural carbon deposits. Possible source of infrared emission from interstellar matter. Prepn: R. Scholl, K. Meyer, Ber. 65, 902 (1932); M. S. Newman, J. Am. Chem. Soc. 62, 1683 (1940). Isoln from coal-hydrogenation oil: M. Orchin, J. Feldman, J. Org. Chem. 18, 609 (1953). UV absorption spectrum: J. W. Patterson, J. Am. Chem. Soc. 64, 1485 (1942). Photophysical properties: R. Katraro et al., Chem. Phys. 42, 121 (1979); N. Nijegorodov et al., Spectrochim. Acta A 57, 2673 (2001). Calorimetry study: Y. Nagano, J. Chem. Thermodyn. 32, 973 (2000). Quantitative structure-property relationships for polycyclic aromatic hydrocarbons: M. M. C. Ferreira, Chemosphere 44, 125 (2001). Thermodynamic properties: J. S. Chickos et al., J. Chem. Thermodyn. 34, 1195 (2002).
Properties: mp 429-430° (Scholl, Meyer). Also reported as pale yellow needles from dilute benzene, mp 437-440° (Newman). bp 590.0°. d 1.39. Soly in water at 25°, log S: -3.85 g/m3.
Melting point: mp 429-430° (Scholl, Meyer); mp 437-440° (Newman)
Boiling point: bp 590.0°
Density: d 1.39
Use: Ultraviolet phosphor for charge-coupled devices.

Others monographs:
NeptuniumMetsulfuron-methylDiacetoneglucoseAluminum Boroformate
Oxygen1,1-DiphenyletheneN2-FormylsulfisomidineCyclobutane
Silver Selenide1-Chloro-2-methyl-1-propeneInfusorial EarthRifamycin SV
TallowArdeparinSerotoninCyclomethycaine
©2016 DrugLead US FDA&EMEA