ⓘ Acenaphthene

                                     

ⓘ Acenaphthene

Acenaphthene is a polycyclic aromatic hydrocarbon consisting of naphthalene with an ethylene bridge connecting positions 1 and 8. It is a colourless solid. Coal tar consists of about 0.3% of this compound.

                                     
  • enzymology, a trans - acenaphthene - 1, 2 - diol dehydrogenase EC 1.10.1.1 is an enzyme that catalyzes the chemical reaction - - trans - acenaphthene - 1, 2 - diol 2
  • Acenaphthoquinone is a quinone derived from acenaphthene It is a water - insoluble yellow solid. It is a precursor to some agrichemicals and dyes. The compound
  • produced industrially by dehydrogenation of acenaphthene Hydrogenation gives the more saturated compound acenaphthene Chemical reduction affords the radical
  • Although structurally a derivative of perylene, it is produced from acenaphthene It is usually applied for cotton fabric, jig dyeing, PVA and silk dyeing
  • The molecular formula C12H10 may refer to: Acenaphthene Benzocyclooctatetraene Biphenyl 1, 3, 5, 7, 9 - Cyclododecapentaen - 11 - yne Dodecatetrayne Elassovalene
  • Structurally, it is a derivative of perylene, although it is produced from acenaphthene It is a less common dye compared to related derivatives such as pigment
  • 2, 3 - derivatives. The 1, 8 - isomer is prepared by aerobic oxidation of acenaphthene 2, 6 - naphthalenedicarboxylic acid can be prepared from this anhydride
  • of pollutants upon receiving waters. Regulated pollutants range from acenaphthene to zinc, with maximum allowed contamination levels in discharge water
  • The compound was originally synthesized by Erich Clar in 1955 from acenaphthene in one method and from chrysene in another. Mitchell and Sondheimer prepared
  • assign a separate taxation category for heat - not - burn tobacco products. Acenaphthene Acetaldehyde Acrylonitrile Acetone Additives non - tobacco Acrolein Aerosol