N16754
2-Nitrofluorene
98%
Synonym(s):
2-Nitro-9H-fluorene
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About This Item
Empirical Formula (Hill Notation):
C13H9NO2
CAS Number:
Molecular Weight:
211.22
MDL number:
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
210-138-5
Product Name
2-Nitrofluorene, 98%
InChI
1S/C13H9NO2/c15-14(16)11-5-6-13-10(8-11)7-9-3-1-2-4-12(9)13/h1-6,8H,7H2
InChI key
XFOHWECQTFIEIX-UHFFFAOYSA-N
SMILES string
[O-][N+](=O)c1ccc-2c(Cc3ccccc-23)c1
assay
98%
form
powder
mp
156-158 °C (lit.)
Quality Level
Related Categories
signalword
Warning
hcodes
Hazard Classifications
Aquatic Chronic 2 - Carc. 2
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type P3 (EN 143) respirator cartridges
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Magdalena Wypij et al.
Molecules (Basel, Switzerland), 25(13) (2020-07-08)
The development of nanotechnology in the last two decades has led to the use of silver nanoparticles (AgNPs) in various biomedical applications, including antimicrobial, anti-inflammatory, and anticancer therapies. However, the potential of the medical application of AgNPs depends on the
X S Cui et al.
Mutation research, 442(1), 9-18 (1999-06-15)
2-Nitrofluorene (NF) is an environmental pollutant. Our previous studies have shown that NF is a carcinogen, primarily targeting the liver, kidney and forestomach in rats. NF-induced DNA adducts were also shown higher levels in the tumor-targeting tissues compared to non-tumor
Weiying Liu et al.
Mutagenesis, 34(2), 165-171 (2018-12-28)
Metabolic activation is essential in standard in vitro genotoxicity test systems. At present, there is a lack of suitable cell models that can express the major characteristics of liver function for predicting substance toxicity in humans. Human-induced hepatocytes (hiHeps), which
Valentina Nanni et al.
Foods (Basel, Switzerland), 9(10) (2020-10-22)
Plant secondary metabolites possess chemopreventive and antineoplastic properties, but the lack of information about their exact mechanism of action in mammalian cells hinders the translation of these compounds in suitable therapies. In light of this, firstly, Origanum vulgare L. hydroalcoholic
W A Kappers et al.
Mutation research, 466(2), 143-159 (2000-03-23)
Three different in vitro mutation assays were used to investigate the involvement of cytochrome P450 enzymes in the activation of the nitro-polycyclic aromatic hydrocarbons (nitroPAHs) 1-nitropyrene and 2-nitrofluorene and their reduced metabolites amino-polycyclic aromatic hydrocarbons (aminoPAHs) 1-aminopyrene and 2-aminofluorene. Mutagenicity
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