N10209
9-硝基蒽
93%
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经验公式（希尔记法）:
C14H9NO2
化学文摘社编号:
分子量:
223.23
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
210-021-9
Beilstein/REAXYS Number:
1877509
MDL number:
Assay:
93%
Form:
powder
InChI key
LSIKFJXEYJIZNB-UHFFFAOYSA-N
InChI
1S/C14H9NO2/c16-15(17)14-12-7-3-1-5-10(12)9-11-6-2-4-8-13(11)14/h1-9H
SMILES string
[O-][N+](=O)c1c2ccccc2cc3ccccc13
assay
93%
form
powder
mp
141-144 °C (lit.)
Quality Level
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存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Karla I Garfias-Gonzalez et al.
Molecules (Basel, Switzerland), 20(5), 8548-8559 (2015-05-20)
Two new classes of dendrimers bearing 8 and 32 fluorene donor groups have been synthesized. The first and second generations of these porphyrin-PAMAM-fluorene dendrimers were characterized by 1H-NMR, 13C-NMR, FTIR, UV-vis spectroscopy, elemental analyses and MALDI-TOF mass spectrometry. The UV-vis
Kazuyuki Mori et al.
Angewandte Chemie (International ed. in English), 54(23), 6847-6851 (2015-04-25)
A single-strand arylene-vinylene precursor containing four phenylene and three naphthylene units linked together with six vinylene spacers undergoes helical folding via sextuple photocyclization to give a [16]helicene core in a single step. The phenylene and naphthylene units are arranged in
9-Nitroanthracene.
IARC monographs on the evaluation of the carcinogenic risk of chemicals to humans, 33, 179-185 (1984-04-01)
Andrea Alparone et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 89, 129-136 (2012-01-20)
Structure, IR and Raman spectra of 1-, 2- and 9-nitroanthracene isomers (1-NA, 2-NA and 9-NA) were calculated and analyzed through density functional theory computations using the B3LYP functional with the 6-311+G** basis set. Steric and π-conjugative effects determine the characteristic
K K Colvert et al.
Biochemical and biophysical research communications, 141(1), 245-250 (1986-11-26)
Xanthine oxidase, a mammalian nitroreductase, catalyzed the covalent binding of a series of nitro-polycyclic aromatic hydrocarbons (nitro-PAHs) trans-dihydrodiols to DNA. Some of the trans-dihydrodiols bound to DNA to a greater extent than their parent nitro-PAHs; however, when the dihydrodiol moiety
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