1-[(4-Nitrophenyl)methyl]pyrazole
- Product Name
- 1-[(4-Nitrophenyl)methyl]pyrazole
- CAS No.
- 110525-57-0
- Chemical Name
- 1-[(4-Nitrophenyl)methyl]pyrazole
- Synonyms
- 1-(4-Nitrobenzyl)pyrazole;1-(4-NITROBENZYL)-1H-PYRAZOLE;1-[(4-Nitrophenyl)methyl]pyrazole;1-(4-NITROBENZYL)-1H-PYRAZOLE, 95+%;1-[(4-nitrophenyl)Methyl]-1H-pyrazole;1H-Pyrazole, 1-[(4-nitrophenyl)methyl]-
- CBNumber
- CB4233970
- Molecular Formula
- C10H9N3O2
- Formula Weight
- 203.2
- MOL File
- 110525-57-0.mol
1-[(4-Nitrophenyl)methyl]pyrazole Property
- Boiling point:
- 394.5±25.0 °C(Predicted)
- Density
- 1.29±0.1 g/cm3(Predicted)
- storage temp.
- Sealed in dry,Room Temperature
- pka
- 1.79±0.10(Predicted)
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H302Harmful if swallowed
H315Causes skin irritation
H319Causes serious eye irritation
H332Harmful if inhaled
H335May cause respiratory irritation
- Precautionary statements
-
P261Avoid breathing dust/fume/gas/mist/vapours/spray.
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
- N495868
- Product name
- 1-(4-Nitrobenzyl)-1H-pyrazole
- Packaging
- 50mg
- Price
- $45
- Updated
- 2021/12/16
- Product number
- N495868
- Product name
- 1-(4-Nitrobenzyl)-1H-pyrazole
- Packaging
- 100mg
- Price
- $60
- Updated
- 2021/12/16
- Product number
- COR0001135
- Product name
- 1-(4-NITROBENZYL)-1H-PYRAZOLE
- Purity
- 95.00%
- Packaging
- 1G
- Price
- $179.55
- Updated
- 2021/12/16
- Product number
- 071890
- Product name
- 1-(4-Nitrobenzyl)-1H-pyrazole
- Purity
- 95+%
- Packaging
- 1g
- Price
- $139
- Updated
- 2021/12/16
- Product number
- 071890
- Product name
- 1-(4-Nitrobenzyl)-1H-pyrazole
- Purity
- 95+%
- Packaging
- 5g
- Price
- $399
- Updated
- 2021/12/16
1-[(4-Nitrophenyl)methyl]pyrazole Chemical Properties,Usage,Production
Synthesis
288-13-1
100-11-8
110525-57-0
A mixture of 4-nitrobenzyl bromide (0.500 g, 2.31 mmol), 1H-pyrazole (0.362 g, 5.23 mmol) and potassium carbonate (0.704 g, 5.09 mmol) in acetonitrile (30 mL) was stirred at room temperature overnight. After completion of the reaction, the reaction mixture was diluted with water and extracted with ethyl acetate (3 × 20 mL). The organic layers were combined, dried over anhydrous sodium sulfate, filtered, and the filtrate concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: hexane/ethyl acetate, gradient elution) to afford 1-[(4-nitrophenyl)methyl]pyrazole (0.380 g, 76% yield) as a white solid. Molecular weight (MW) = 203.20. 1H NMR (CDCl3, 500 MHz) δ 8.21-8.19 (m, 1H), 8.19-8.16 (m, 1H), 7.61-7.57 (m, 1H), 7.48-7.44 (m, 1H), 7.32-7.28 (m, 2H), 6.35 (t, J = 2.1 Hz. 1H), 5.44 (s, 2H); APCI MS m/z 204 [M + H]+.
References
[1] Organic Preparations and Procedures International, 2000, vol. 32, # 4, p. 385 - 390
[2] Patent: WO2014/66659, 2014, A1. Location in patent: Paragraph 0824
1-[(4-Nitrophenyl)methyl]pyrazole Preparation Products And Raw materials
Raw materials
Preparation Products
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