m-nitroanisole

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Names

[ CAS No. ]:
555-03-3

[ Name ]:
m-nitroanisole

[Synonym ]:
3-nitro-anisole
3-Nitroanisole
m-methoxynitrobenzene
3-Methoxynitrobenzene
3-nitromethoxybenzene
Anisole,m-nitro
EINECS 209-079-8
Methyl 3-nitrophenyl ether
m-nitroanisole
META-NITROANISOLE
1-Methoxy-3-nitrobenzene
MFCD00007237
3-Nitrophenylmethylether
Benzene, 1-methoxy-3-nitro-
m-MeOC6H4NO2
1-methoxy-3-nitro-benzen

Chemical & Physical Properties

[ Density]:
1.2±0.1 g/cm3

[ Boiling Point ]:
256.3±13.0 °C at 760 mmHg

[ Melting Point ]:
36-38°C

[ Molecular Formula ]:
C7H7NO3

[ Molecular Weight ]:
153.135

[ Flash Point ]:
127.9±21.8 °C

[ Exact Mass ]:
153.042587

[ PSA ]:
55.05000

[ LogP ]:
2.17

[ Vapour Pressure ]:
0.0±0.5 mmHg at 25°C

[ Index of Refraction ]:
1.543

[ Storage condition ]:
2-8°C

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H302

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xn:Harmful;

[ Risk Phrases ]:
R22

[ Safety Phrases ]:
S24/25

[ RIDADR ]:
3458

[ RTECS ]:
BZ8787000

[ Packaging Group ]:
III

[ Hazard Class ]:
6.1(b)

[ HS Code ]:
29093090

Customs

[ HS Code ]: 2909309090

[ Summary ]:
2909309090 other aromatic ethers and their halogenated, sulphonated, nitrated or nitrosated derivatives VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:5.5% General tariff:30.0%

Articles

Spectroscopic and kinetic study of the photoinduced methoxy substitution of 3-nitroanisole and 3, 5-dinitroanisole. Van Zeijl PHM, et al.

J. Photochem. 29(3) , 415-33, (1985)

Nitrophenyl ethers as possible photoaffinity labels. The nucleophilic aromatic photosubstitution revisited. Cerveló J., et al.

Tetrahedron Lett. 25(37) , 4147-50, (1984)

Modification of an intermolecular photoreaction by cyclodextrin: the photohydroxylation of 3-nitroanisole. Evans CH and Gunnlaugsson T.

J. Photochem. Photobiol. A: Chem. 78(1) , 57-62, (1994)


More Articles

Related Compounds

  • m-PEG2-O-Ph-3-NH2
  • m-trifluoromethylbenzyl nitrate
  • m-PEG-acid
  • m-Chlorbenzyl chloride
  • m-Terphenyl
  • m-dhbppe
  • 2-({1-[(Oxolan-3-yl)methyl]piperidin-3-yl}methoxy)pyrimidine
  • 1-Methyl-3-{3-[(pyrimidin-2-yloxy)methyl]piperidin-1-yl}pyrrolidin-2-one
  • 4-(2-{3-[(Pyrimidin-2-yloxy)methyl]piperidin-1-yl}ethyl)-1,4-oxazepan-5-one
  • 2-({1-[3-(Trifluoromethyl)-[1,2,4]triazolo[4,3-b]pyridazin-6-yl]piperidin-3-yl}methoxy)pyridine-4-carbonitrile
  • 1-Methyl-3-(3-{[(6-methylpyridin-2-yl)oxy]methyl}piperidin-1-yl)-1,2-dihydropyrazin-2-one
  • 5-Bromo-2-(3-{[(6-methylpyridin-2-yl)oxy]methyl}piperidin-1-yl)pyrimidine
  • 5-Fluoro-2-(3-{[(6-methylpyridin-2-yl)oxy]methyl}piperidin-1-yl)pyrimidine
  • 5-Chloro-2-(3-{[(6-methylpyridin-2-yl)oxy]methyl}piperidin-1-yl)pyrimidine
  • 2-Methyl-6-({1-[3-(trifluoromethyl)-[1,2,4]triazolo[4,3-b]pyridazin-6-yl]piperidin-3-yl}methoxy)pyridine
  • 2-(3-{[(6-Methylpyridin-2-yl)oxy]methyl}piperidin-1-yl)-4-(trifluoromethyl)pyrimidine
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