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Merck
모든 사진(2)

주요 문서

236284

Sigma-Aldrich

2-Nitroanisole

≥99%

동의어(들):

1-Methoxy-2-nitrobenzene

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About This Item

Linear Formula:
O2NC6H4OCH3
CAS Number:
Molecular Weight:
153.14
Beilstein:
1868032
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

분석

≥99%

양식

liquid

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.)

작용기

nitro

SMILES string

COc1ccccc1[N+]([O-])=O

InChI

1S/C7H7NO3/c1-11-7-5-3-2-4-6(7)8(9)10/h2-5H,1H3

InChI key

CFBYEGUGFPZCNF-UHFFFAOYSA-N

유사한 제품을 찾으십니까? 방문 제품 비교 안내

일반 설명

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.

애플리케이션

2-Nitroanisole has been employed as solvatochromic probe to examine cybotactic region of pure and mixed supercritical fluid solvent systems.

픽토그램

Health hazardExclamation mark

신호어

Danger

유해 및 위험 성명서

Hazard Classifications

Acute Tox. 4 Oral - Carc. 1B

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

개인 보호 장비

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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시험 성적서(COA)

Lot/Batch Number

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문서 라이브러리에서 최근에 구매한 제품에 대한 문서를 찾아보세요.

문서 라이브러리 방문

Characterization of supercritical fluid solvents using solvatochromic shifts.
Yonker CR, et al.
The Journal of Physical Chemistry, 90(13), 3022-3026 (1986)
Mohammad Asaduzzaman Miah et al.
Ecology and evolution, 7(14), 5032-5040 (2017-08-05)
Cytochrome P450 monooxygenases (CYPs) usually overexpressed in resistant strain were found involved in oxidative detoxification of insecticides. In this study, an investigation was conducted to confirm if resistance irrelevant CYPs which were not overexpressed in resistant strain before, were capable
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
Effects of physical binding of o-Nitroanisole with feed upon its systemic availability in male F344 rats.
J H Yuan et al.
Bulletin of environmental contamination and toxicology, 47(1), 152-159 (1991-07-01)
R D Irwin et al.
Fundamental and applied toxicology : official journal of the Society of Toxicology, 30(1), 1-12 (1996-03-01)
o-Nitroanisole, a mutagenic intermediate used in the manufacture of azo dyes, was administered in feed for 2 years at concentrations of 0, 222, 666, or 2000 ppm to groups of 60 male and 60 female F344 rats. No significant increase

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