ChemicalBook > CAS DataBase List > 1-Benzyl-4-nitro-1H-pyrazole

1-Benzyl-4-nitro-1H-pyrazole

Product Name
1-Benzyl-4-nitro-1H-pyrazole
CAS No.
88095-61-8
Chemical Name
1-Benzyl-4-nitro-1H-pyrazole
Synonyms
1-Benzyl-4-nitropyrazole;1-Benzyl-4-nitro-1H-pyrazole;4-nitro-1-(phenylmethyl)pyrazole;1H-Pyrazole,4-nitro-1-(phenylmethyl)-
CBNumber
CB91262189
Molecular Formula
C10H9N3O2
Formula Weight
203.2
MOL File
88095-61-8.mol
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1-Benzyl-4-nitro-1H-pyrazole Property

Melting point:
56-58°C
Boiling point:
379.9±25.0 °C(Predicted)
Density 
1.29±0.1 g/cm3(Predicted)
storage temp. 
2-8°C
pka
-2.31±0.10(Predicted)
Appearance
White to off-white Solid
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Safety

Hazard Codes 
Xi
HazardClass 
IRRITANT
HS Code 
2933199090
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

Precautionary statements

P280Wear protective gloves/protective clothing/eye protection/face protection.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
L119733
Product name
1-BENZYL-4-NITRO-1H-PYRAZOLE
Purity
AldrichCPR
Packaging
10MG
Price
$30.7
Updated
2025/07/31
Biosynth Carbosynth
Product number
FB130298
Product name
1-Benzyl-4-nitro-1H-pyrazole
Packaging
250mg
Price
$85
Updated
2021/12/16
Biosynth Carbosynth
Product number
FB130298
Product name
1-Benzyl-4-nitro-1H-pyrazole
Packaging
500mg
Price
$150
Updated
2021/12/16
SynQuest Laboratories
Product number
4H54-1-7U
Product name
1-Benzyl-4-nitro-1H-pyrazole
Packaging
1g
Price
$192
Updated
2021/12/16
AK Scientific
Product number
V8576
Product name
1-Benzyl-4-nitropyrazole
Packaging
10g
Price
$200
Updated
2021/12/16
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1-Benzyl-4-nitro-1H-pyrazole Chemical Properties,Usage,Production

Synthesis

2075-46-9

100-39-0

88095-61-8

a) Under argon protection, 4-nitro-1H-pyrazole (283 mg, 2.5 mmol) was dissolved in anhydrous DMF (5 mL), followed by the addition of NaH (120 mg, 2.75 mmol). The reaction mixture was stirred at 0 °C for 1 h, then cooled to 0 °C again and benzyl bromide (300 μL, 2.5 mmol) was added dropwise. Subsequently, the reaction mixture was stirred at room temperature for 12 hours. After completion of the reaction, the reaction mixture was diluted with water and extracted with ethyl acetate. The organic phases were combined and purified by silica gel column chromatography using heptane/ethyl acetate as eluent. The final product was 1-benzyl-4-nitro-1H-pyrazole as a light yellow oil (484 mg, 95% yield). Mass spectral analysis (ISP, m/e): 226.3 (100) [(M + Na)+].

References

[1] Journal of Medicinal Chemistry, 2014, vol. 57, # 13, p. 5714 - 5727
[2] Patent: US2010/120874, 2010, A1. Location in patent: Page/Page column 27-28

1-Benzyl-4-nitro-1H-pyrazole Preparation Products And Raw materials

Raw materials

Preparation Products

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1-Benzyl-4-nitro-1H-pyrazole Suppliers

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