N10209
9-Nitroanthracene
93%
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About This Item
Empirical Formula (Hill Notation):
C14H9NO2
CAS Number:
Molecular Weight:
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
Quality Level
mp
141-144 °C (lit.)
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Related Categories
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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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
P P Fu et al.
Carcinogenesis, 6(5), 753-757 (1985-05-01)
Aerobic metabolism of 9-nitroanthracene by uninduced rat liver microsomes produced four metabolites identified as trans-1,2- and 3,4-dihydrodiols, 1,2,3,4-tetrahydrotetrol of 9-nitroanthracene, and anthraquinone. Further metabolism of the predominant metabolite, 9-nitroanthracene trans-3,4-dihyrodiol, yielded a 1,2,3,4-tetrahydrotetrol with a trans-cis-trans configuration, indicating that a
Kiyoshi Fukuhara et al.
Bioorganic & medicinal chemistry, 15(11), 3869-3873 (2007-04-03)
Anthraquinones are typical photosensitizers used in photodynamic therapy (PDT). However, systemic toxicity is a major problem for anthraquinones due to their ability not only to bind DNA but also to cause oxidative stress even without photoirradiation. To avoid such disadvantages
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
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