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
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
Safety
- Hazard Codes
- Xi
- HazardClass
- IRRITANT
- HS Code
- 2933199090
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.
N-Bromosuccinimide Price
- Product number
- L119733
- Product name
- 1-BENZYL-4-NITRO-1H-PYRAZOLE
- Purity
- AldrichCPR
- Packaging
- 10MG
- Price
- $30.7
- Updated
- 2025/07/31
- Product number
- FB130298
- Product name
- 1-Benzyl-4-nitro-1H-pyrazole
- Packaging
- 250mg
- Price
- $85
- Updated
- 2021/12/16
- Product number
- FB130298
- Product name
- 1-Benzyl-4-nitro-1H-pyrazole
- Packaging
- 500mg
- Price
- $150
- Updated
- 2021/12/16
- Product number
- 4H54-1-7U
- Product name
- 1-Benzyl-4-nitro-1H-pyrazole
- Packaging
- 1g
- Price
- $192
- Updated
- 2021/12/16
- Product number
- V8576
- Product name
- 1-Benzyl-4-nitropyrazole
- Packaging
- 10g
- Price
- $200
- Updated
- 2021/12/16
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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