3-Methyl-4-nitropyrazole

3-Methyl-4-nitropyrazole Suppliers list
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Products Intro: Product Name:3-Methyl-4-nitropyrazole
CAS:5334-39-4
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CAS:5334-39-4
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CAS:5334-39-4
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CAS:5334-39-4
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Products Intro: Product Name:3-Methyl-4-nitropyrazole
CAS:5334-39-4
Purity:99.0% Package:100g;1kg;5kg;25kg

3-Methyl-4-nitropyrazole manufacturers

3-Methyl-4-nitropyrazole Basic information
Uses
Product Name:3-Methyl-4-nitropyrazole
Synonyms:3-Methyl-4-Nitro-1H-Pyrazole;at-7519-lua2-3-261-156g;1H-Pyrazole,3-methyl-4-nitro-(9CI);3-Methyl-4-nitropyrazole;3-Methyl-4-nitropyra;3-Methyl-4-Nitro-1H-Pyrazole;3-Methyl-4-nitropyrazole>;1H-Pyrazole, 3-methyl-4-nitro-
CAS:5334-39-4
MF:C4H5N3O2
MW:127.1
EINECS:
Product Categories:NITRO
Mol File:5334-39-4.mol
3-Methyl-4-nitropyrazole Structure
3-Methyl-4-nitropyrazole Chemical Properties
Melting point 131-134℃
Boiling point 325℃
density 1.426±0.06 g/cm3(Predicted)
RTECS UQ7435000
storage temp. Sealed in dry,Room Temperature
form powder to crystal
pka10.19±0.50(Predicted)
color White to Light yellow
Water Solubility Slightly soluble in water.
InChIInChI=1S/C4H5N3O2/c1-3-4(7(8)9)2-5-6-3/h2H,1H3,(H,5,6)
InChIKeyWTZYTQJELOHMMJ-UHFFFAOYSA-N
SMILESN1C=C([N+]([O-])=O)C(C)=N1
Safety Information
Risk Statements 36/37/38
Safety Statements 26-37
HS Code 29331990
MSDS Information
3-Methyl-4-nitropyrazole Usage And Synthesis
Uses

3-Methyl-4-nitropyrazole is a reactant used in the preparation of aminopyrazole derivatives as potent, selective and brain penetrant Leucine-rich repeat kinase 2(LRRK2) small molecule inhibitors.

Uses3-Methyl-4-nitropyrazole is a reactant used in the preparation of aminopyrazole derivatives as potent, selective and brain penetrant Leucine-rich repeat kinase 2(LRRK2) small molecule inhibitors.
Synthesis
3-Methyl-4-iodopyrazole

15802-75-2

3-Methyl-4-nitropyrazole

5334-39-4

General method: 3-methyl-4-iodopyrazole (1 mmol) was dissolved in tetrahydrofuran (THF, 10 mL) and Fuajasite catalyst (250 mg) was added. Concentrated nitric acid (density 1.52 g/cm3, 10 mL) was added slowly and the reaction was stirred at room temperature until completion. At the end of the reaction, the catalyst was removed by filtration and the filtrate was extracted with dichloromethane several times. The organic phases were combined and concentrated under reduced pressure to remove the solvent to obtain 3-methyl-4-nitropyrazole.

References[1] Synthetic Communications, 2012, vol. 42, # 23, p. 3463 - 3471
[2] Catalysis Communications, 2013, vol. 42, p. 35 - 39
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