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1-NITROPYRAZOLE

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1-NITROPYRAZOLE Basic information

Product Name:
1-NITROPYRAZOLE
Synonyms:
  • 1-NITROPYRAZOLE
  • 1-NITRO-1H-PYRAZOLE
  • AKOS B006480
  • TIMTEC-BB SBB000027
  • 1H-Pyrazole, 1-nitro-
  • 1H-Pyrazole,1-nitro-(9CI)
  • N-Nitropyrazole
  • 1-Nitopyrazole
CAS:
7119-95-1
MF:
C3H3N3O2
MW:
113.07
Product Categories:
  • Building Blocks
  • Heterocyclic Building Blocks
  • Pyrazoles
  • NITRO
  • Heterocyclic Compounds
Mol File:
7119-95-1.mol
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1-NITROPYRAZOLE Chemical Properties

Melting point:
92-94 °C(lit.)
Boiling point:
269°C
Density 
1.55±0.1 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
form 
powder to crystal
pka
-5.04±0.12(Predicted)
color 
White to Light yellow
CAS DataBase Reference
7119-95-1(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xn
Risk Statements 
22-36/37/38
Safety Statements 
22-26-36
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
2933199090

MSDS

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1-NITROPYRAZOLE Usage And Synthesis

Synthesis

288-13-1

7119-95-1

The general procedure for the synthesis of 1-nitropyrazole from pyrazole was as follows: first, the nitroxide was prepared by slowly mixing acetic anhydride with fuming nitric acid at a volume ratio of 5.5:1 under ice-water bath conditions. Subsequently, the nitroxide and the acetic acid solution of pyrazole were fed into the microchannel reactor at a precisely controlled flow rate (0.1 mL/min for the pyrazole acetic acid solution), respectively, via a high-pressure delivery system. In this process, a constant flow pump was used to ensure that the molar ratio of nitric acid to pyrazole was strictly controlled at 1.1:1. The reaction was carried out in the microchannel reactor at a temperature maintained at 45-70 °C to achieve instantaneous mixing and reaction of the two liquids. Upon completion of the reaction, the reaction liquid was quenched by pouring it into crushed ice and the products were separated by filtration. The product was washed with ice water and dried under vacuum to give the final N-nitropyrazole. The yield and purity data of the products are detailed in Table 1 and Figure 2.

References

[1] Patent: CN108570010, 2018, A. Location in patent: Paragraph 0035; 0036; 0037; 0038; 0041-0070
[2] Archiv der Pharmazie, 1995, vol. 328, # 4, p. 349 - 358
[3] ChemPlusChem, 2018, vol. 83, # 8, p. 804 - 811
[4] Journal of Chemical Research - Part S, 1996, # 5, p. 244 - 245
[5] Beilstein Journal of Organic Chemistry, 2013, vol. 9, p. 1517 - 1525

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