Basic information Safety Supplier Related

2-METHYL-4-NITRO-2H-PYRAZOLE-3-CARBOXYLIC ACID

Basic information Safety Supplier Related

2-METHYL-4-NITRO-2H-PYRAZOLE-3-CARBOXYLIC ACID Basic information

Product Name:
2-METHYL-4-NITRO-2H-PYRAZOLE-3-CARBOXYLIC ACID
Synonyms:
  • ART-CHEM-BB B000133
  • TIMTEC-BB SBB000165
  • AKOS B000133
  • 2-METHYL-4-NITRO-2H-PYRAZOLE-3-CARBOXYLIC ACID
  • 1-METHYL-4-NITRO-1H-PYRAZOLE-5-CARBOXYLIC ACID
  • 1-METHYL-4-NITRO-5-PYRAZOLECARBOXYLIC ACID
  • 1-methyl-4-nitro-1H-pyrazole-5-carboxylic acid(SALTDATA: FREE)
  • 2-methyl-4-nitropyrazole-3-carboxylic acid
CAS:
92534-69-5
MF:
C5H5N3O4
MW:
171.11
Mol File:
Mol File
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2-METHYL-4-NITRO-2H-PYRAZOLE-3-CARBOXYLIC ACID Chemical Properties

Melting point:
160-161°C
Boiling point:
399.0±27.0 °C(Predicted)
Density 
1.72±0.1 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
pka
2.10±0.50(Predicted)
Appearance
White to off-white Solid
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Safety Information

Hazard Codes 
Xi
HazardClass 
IRRITANT
HS Code 
2933199090
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2-METHYL-4-NITRO-2H-PYRAZOLE-3-CARBOXYLIC ACID Usage And Synthesis

Synthesis

16034-46-1

92534-69-5

The general procedure for the synthesis of 1-methyl-4-nitro-pyrazole-5-carboxylic acid from 1-methyl-1H-pyrazole-5-carboxylic acid was as follows: fuming sulfuric acid (1977 mmol) was slowly added dropwise to fuming nitric acid (777 mmol) under strictly controlled temperature conditions. Subsequently, 1-methyl-1H-pyrazole-5-carboxylic acid (277 mmol) was added in batches to ensure that the reaction temperature was maintained below 60 °C. The reaction was carried out at the same temperature. After the addition was completed, the reaction mixture was stirred continuously at the same temperature for 1 hour. Upon completion of the reaction, the mixture was quenched by careful pouring into crushed ice and extracted with ethyl acetate (300 mL x 3). The organic phases were combined, washed sequentially with water (250 mL x 2) and dried with anhydrous sodium sulfate. Finally, the solvent was removed by distillation under reduced pressure to afford 1-methyl-4-nitro-pyrazole-5-carboxylic acid as a light yellow solid in a yield of 23.6 g in 50% yield. [00251] 1H NMR (400 MHz, DMSO-d6) δ: 8.29 (1H, s); 3.95 (3H, s).

References

[1] Chemistry of Heterocyclic Compounds (New York, NY, United States), 1983, vol. 19, # 12, p. 1326 - 1330
[2] Khimiya Geterotsiklicheskikh Soedinenii, 1983, vol. 19, # 12, p. 1676 - 1679
[3] Journal of Organic Chemistry USSR (English Translation), 1984, vol. 20, # 5, p. 976 - 980
[4] Zhurnal Organicheskoi Khimii, 1984, vol. 20, # 5, p. 1073 - 1078
[5] Patent: WO2009/71705, 2009, A1. Location in patent: Page/Page column 39

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