236284
2-硝基苯甲醚
≥99%
别名:
1-甲氧基-2-硝基苯
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关于此项目
线性分子式:
O2NC6H4OCH3
化学文摘社编号:
分子量:
153.14
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-052-1
Beilstein/REAXYS Number:
1868032
MDL number:
Assay:
≥99%
Form:
liquid
InChI key
CFBYEGUGFPZCNF-UHFFFAOYSA-N
InChI
1S/C7H7NO3/c1-11-7-5-3-2-4-6(7)8(9)10/h2-5H,1H3
SMILES string
COc1ccccc1[N+]([O-])=O
assay
≥99%
form
liquid
Quality Level
refractive index
n20/D 1.561 (lit.)
bp
273 °C (lit.)
mp
9-12 °C (lit.)
solubility
alcohol: soluble(lit.), diethyl ether: soluble(lit.), water: insoluble(lit.)
density
1.254 g/mL at 25 °C (lit.)
functional group
nitro
General description
2-Nitroanisole (2-methoxynitrobenzene is an industrial and environmental pollutant causing tumors of the urinary bladder in rats and mice. Tumorigenic potential of 2-nitroanisole has been evaluated by host-mediated in vitro and in vivo assay.
Application
2-Nitroanisole has been employed as solvatochromic probe to examine cybotactic region of pure and mixed supercritical fluid solvent systems.
wgk
WGK 3
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Carc. 1B
存储类别
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
危险化学品
此项目有
A Esmaeili et al.
Anticancer research, 26(6B), 4203-4212 (2007-01-05)
The host-mediated in vitro/in vivo assay system was used to evaluate the tumorigenic potential of the aromatic nitro compound 2-nitroanisole (2-NA). After intraperitoneal administration of the compound, resident macrophages were recovered by peritoneal lavage from treated and untreated mice and
T Prabhu et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 83(1), 8-16 (2011-10-04)
Fourier-transform Raman and infrared spectra of 2-nitroanisole are recorded (4000-100 cm(-1)) and interpreted by comparison with respective theoretical spectra calculated using HF and DFT method. The geometrical parameters with C(S) symmetry, harmonic vibrational frequencies, infrared and Raman scattering intensities are
Y Miura et al.
Comparative biochemistry and physiology. B, Comparative biochemistry, 100(2), 249-252 (1991-01-01)
1. The cytochrome P-450 content (0.75 +/- 0.13 nmol/mg microsomal protein) in musk shrew (suncus, Suncus murinus) liver microsomes was lower than that (1.30 +/- 0.26) in rat liver microsomes, but it is approximately the same level as in the
Markéta Miksanová et al.
Chemical research in toxicology, 17(5), 663-671 (2004-05-18)
2-Nitroanisole (2-NA) is an important industrial pollutant and a potent carcinogen for rodents. Determining the capability of humans to metabolize 2-NA and understanding which human cytochrome P450 (P450) enzymes are involved in its activation and/or detoxification are important to assess
Marie Stiborová et al.
Interdisciplinary toxicology, 2(1), 24-27 (2009-03-01)
An aromatic amine, o-anisidine (2-methoxyaniline) and its oxidative counterpart, 2-nitroanisole (2-methoxynitrobenzene), are the industrial and environmental pollutants causing tumors of the urinary bladder in rats and mice. Both carcinogens are activated to the same proximate carcinogenic metabolite, N-(2-methoxyphenyl)hydroxylamine, which spontaneously
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