1-Nitronaphthalene

1-nitronaphthalene 200.svg 1-nitronaphthalene.jpg 120 px 1-Nitronaphthalene α-Nitronaphthalene 86-57-7 1867714 34104 165373 6588 DTXSID7020978 201-684-5 C14040 6849 2538 A51NP1DL2T 1S/C10H7NO2/c12-11(13)10-7-3-5-8-4-1-2-6-9(8)10/h1-7H RJKGJBPXVHTNJL-UHFFFAOYSA-N C1=CC=C2C(=C1)C=CC=C2[N+](=O)[O-] 10 7 1 2 pale yellow solid 1.223 g/cm3 53-57 304 releases toxic and flammable gas 0.00064 hPa none 103594 1-nitronapthalene 22 October 2025 02 07 09 Warning 228 302 411 210 240 241 264 270 273 280 301+312+330 370+378 391 501 4 2 2 W Safety Data Sheet - 1-nitronapthalene https://www.fishersci.com/store/msds?partNumber=AC147040050&productDescription=1-NITRONAPHTHALENE+99%25+5G&vendorId=VN00032119&countryCode=US&language=en FisherSci.com ThermoFisher Scientific 22 October 2025 24 December 2021 164 (closed cup) 450 350 mg/kg (oral, rat) >0.04 mg/L (inhalation, rat) 2.0 - 4.0 mg/L (fathead minnow, 96h) 1-Nitronaphthalene is an organic compound with the formula C10H7NO2. It is one of two isomers of nitronaphthalene. A pale yellow, sublimable solid, 1-nitronaphthalene is the main product of the direct nitration of naphthalene. It is an intermediate in the production of naphthylamine, a precursor to dyes.10.1002/14356007.a17_411 Nitro Compounds, Aromatic 2005 Booth Gerald The conversion to the amine is effected by hydrogenation.10.1038/nchem.1645 Heterogenized Cobalt Oxide Catalysts for Nitroarene Reduction by Pyrolysis of Molecularly Defined Complexes 2013 Westerhaus Felix A. Jagadeesh Rajenahally V. Wienhöfer Gerrit Pohl Marga-Martina Radnik Jörg Surkus Annette-Enrica Rabeah Jabor Junge Kathrin Junge Henrik Nielsen Martin Brückner Angelika Beller Matthias Nature Chemistry 5 6 537–543 23695637 2013NatCh...5..537W 3273484 References Category:Nitronaphthalenes Category:1-Naphthyl compounds