3,5-dibromo-1-methyl-4-nitro-1H-pyrazole

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3,5-dibromo-1-methyl-4-nitro-1H-pyrazole Basic information
Product Name:3,5-dibromo-1-methyl-4-nitro-1H-pyrazole
Synonyms:3,5-dibromo-1-methyl-4-nitro-1H-pyrazole;1H-Pyrazole, 3,5-dibromo-1-methyl-4-nitro-
CAS:155600-99-0
MF:C4H3Br2N3O2
MW:284.89
EINECS:
Product Categories:
Mol File:155600-99-0.mol
3,5-dibromo-1-methyl-4-nitro-1H-pyrazole Structure
3,5-dibromo-1-methyl-4-nitro-1H-pyrazole Chemical Properties
Melting point 153-155°
Boiling point 279.1±35.0 °C(Predicted)
density 2.51±0.1 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
pka-5.83±0.10(Predicted)
Safety Information
HazardClass IRRITANT
MSDS Information
3,5-dibromo-1-methyl-4-nitro-1H-pyrazole Usage And Synthesis
Synthesis
3,5-dibromo-4-nitro-1H-pyrazole

104599-36-2

3,5-dibromo-1-methyl-4-nitro-1H-pyrazole

155600-99-0

Example A: Steps for the synthesis of 3,5-dibromo-1-methyl-4-nitro-1H-pyrazole (2): 1. dissolve 3,5-dibromo-4-nitropyrazole (1) (0.934 g, 3.45 mmol) in 5 mL of anhydrous DMF under dry conditions. 2. 100 mL of DMF solution containing 0.16 g of sodium hydride (6.67 mmol) was slowly added dropwise to the above solution over a period of 1 hour. 3. 0.26 mL of iodomethane (CH3I, 3.89 mmol) was added dropwise to the reaction system after gas release ceased. 4. The reaction mixture was stirred at room temperature overnight. 5. Upon completion of the reaction, the solvent was removed by vacuum evaporation. 6. The residue was poured into water and the solid product was separated by filtration. 7. 7. The solid was washed with water and dried under vacuum to give 0.713 g of the target compound 2 in 72.6% yield.

References[1] Patent: US2009/282622, 2009, A1
3,5-dibromo-1-methyl-4-nitro-1H-pyrazole Preparation Products And Raw materials
Raw materials3,5-dibromo-4-nitro-1H-pyrazole-->N,N-Dimethylformamide
Tag:3,5-dibromo-1-methyl-4-nitro-1H-pyrazole(155600-99-0) Related Product Information
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