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ChemicalBook--->CAS DataBase List--->1074-98-2

1074-98-2

1074-98-2 Structure

1074-98-2 Structure
IdentificationMore
[Name]

4-Nitro-3-picoline N-oxide
[CAS]

1074-98-2
[Synonyms]

3-METHYL-4-NITROPYRIDINE 1-OXIDE
3-METHYL-4-NITROPYRIDINE N-OXIDE
4-NITRO-3-PICOLINE N-OXIDE
3-methyl-4-nitro-pyridin1-oxide
3-Picoline, 4-nitro-, 1-oxide
4-Nitro-3-methylpyridine N-oxide
4-Nitro-3-picoline 1-oxide
4-Nitro-beta-picoline N-oxide
5-Methyl-4-nitropyridine N-oxide
Pyridine, 3-methyl-4-nitro-, 1-oxide
3-METHYL-4-NITROPYRIDINE N-OXIDE 98%
4-Nitro-3-picoline-N-oxide 99%
4-Nitro-B-picoline N-oxide
[EINECS(EC#)]

214-050-8
[Molecular Formula]

C6H6N2O3
[MDL Number]

MFCD00014626
[Molecular Weight]

154.12
[MOL File]

1074-98-2.mol
Chemical PropertiesBack Directory
[Appearance]

yellow crystalline needles or powder
[Melting point ]

135-139 °C
[Boiling point ]

277.46°C (rough estimate)
[density ]

1.4564 (rough estimate)
[refractive index ]

1.5100 (estimate)
[storage temp. ]

2-8°C
[form ]

Crystalline Needles or Powder
[pka]

-1.22±0.10(Predicted)
[color ]

Yellow
[BRN ]

140157
[InChI]

InChI=1S/C6H6N2O3/c1-5-4-7(9)3-2-6(5)8(10)11/h2-4H,1H3
[InChIKey]

SSOURMYKACOBIV-UHFFFAOYSA-N
[SMILES]

C1[N+]([O-])=CC=C([N+]([O-])=O)C=1C
[CAS DataBase Reference]

1074-98-2(CAS DataBase Reference)
[NIST Chemistry Reference]

4-Nitro-3-picoline-n-oxide(1074-98-2)
Safety DataBack Directory
[Hazard Codes ]

Xn,Xi
[Risk Statements ]

R40:Limited evidence of a carcinogenic effect.
R20/21/22:Harmful by inhalation, in contact with skin and if swallowed .
R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) .
S36/37:Wear suitable protective clothing and gloves .
S36:Wear suitable protective clothing .
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S22:Do not breathe dust .
[RIDADR ]

2811
[WGK Germany ]

3
[RTECS ]

UT5775000
[Hazard Note ]

Irritant/Possible Mutagen
[HazardClass ]

6.1
[PackingGroup ]

II
[HS Code ]

29333990
Raw materials And Preparation ProductsBack Directory
[Raw materials]

3-Methyl-4-nitropyridine-->Dichloromethane-->Sulfuric acid-->3-Picoline-->3-Picoline-N-oxide-->Nitric acid
[Preparation Products]

5-Azaindole-->4-Chloro-3-methylpyridine-->4-Bromo-3-methylpyridine-->4(1H)-Pyridinimine, 3-methyl--->Acetamide, N-(3-methyl-4-pyridinyl)- (9CI)-->4-methoxy-3-methylpyridine N-oxide
Material Safety Data Sheet(MSDS)Back Directory
[msds information]

3-Methyl-4-nitropyridine-1-oxide(1074-98-2).msds
Hazard InformationBack Directory
[Chemical Properties]

yellow crystalline needles or powder
[General Description]

3-Methyl-4-nitropyridine N-Oxide (POM) is an efficient nonlinear optical organic material having a high nonlinear coefficient and achieving the parametric emission process within the desired spectral range (1–2 μm). POM crystallizes in the orthorhombic class, space group P212121, and point group 222. It is a positive biaxial crystal. It melts at 136°C and the nonlinear coefficient is deff=10 pm/V[1]. This compound exhibits a negative-linear-compressibility (NLC) region as well as exceptionally large positive thermal expansion. The initial compression of the weak supramolecular network in the molecular POM crystal is analogous to the hydrostatic responses of the framework crystals with much stronger cohesion forces. 3-Methyl-4-nitropyridine N-Oxide is a commercial NLO material for pico- and femtosecond optics in the near-IR range[2].
[Synthesis]

Nitration of picoline-N-oxide in the fourth position yields 3-Methyl-4-nitropyridine N-Oxide. Initially, Picoline-N-oxide (50 g) was melted at 38C and mixed with sulfuric acid (250 ml) in cold condition. Later, nitration of this mixture was done at room temperature by addition of sodium nitrate (70 g) and the solution was continuously stirred until all the solid particles dissolves. Temperature was increased slowly to 70C by keeping it in an oil bath and solution was stirred continuously for 2 h at this temperature. To ensure complete nitration, the solution was maintained about 95–100C for 12 h with continuous stirring. The reaction mixture was taken out from the oil bath and cooled. It is then poured over crushed ice and neutralized with ammonia solution till the pH reaches about 7–8. On cooling, bright yellow crystalline 3-Methyl-4-nitropyridine N-Oxide powder was obtained. It was washed and dried in vacuum[1].
[References]

[1] Boomadevi, S. , H. P. Mittal , and R. Dhansekaran . "Synthesis, crystal growth and characterization of 3-methyl 4-nitropyridine 1-oxide (POM) single crystals."Journal of Crystal Growth 261.1(2004):55-62.
[2] Cai, Weizhao , et al. "Anomalous compression of a weakly CHO bonded nonlinear optical molecular crystal." Journal of Materials Chemistry C 2.32(2014).
Spectrum DetailBack Directory
[Spectrum Detail]

4-Nitro-3-picoline N-oxide(1074-98-2)MS
4-Nitro-3-picoline N-oxide(1074-98-2)1HNMR
4-Nitro-3-picoline N-oxide(1074-98-2)13CNMR
4-Nitro-3-picoline N-oxide(1074-98-2)IR1
4-Nitro-3-picoline N-oxide(1074-98-2)IR2
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

3-Methyl-4-nitropyridine N-oxide, 98%(1074-98-2)
[Alfa Aesar]

4-Nitro-3-picoline N-oxide, 98%(1074-98-2)
[Sigma Aldrich]

1074-98-2(sigmaaldrich)
[TCI AMERICA]

4-Nitro-3-picoline N-Oxide,>97.0%(T)(1074-98-2)
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