ChemicalBook > CAS DataBase List > 1-(3-nitrophenyl)-1H-pyrazole

1-(3-nitrophenyl)-1H-pyrazole

Product Name
1-(3-nitrophenyl)-1H-pyrazole
CAS No.
25688-18-0
Chemical Name
1-(3-nitrophenyl)-1H-pyrazole
Synonyms
1-(3-nitrophenyl)-1H-pyrazole;1H-Pyrazole, 1-(3-nitrophenyl)-
CBNumber
CB52593806
Molecular Formula
C9H7N3O2
Formula Weight
189.17
MOL File
25688-18-0.mol
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1-(3-nitrophenyl)-1H-pyrazole Property

Melting point:
94.5-95 °C
Boiling point:
323.6±25.0 °C(Predicted)
Density 
1.33±0.1 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
pka
-0.60±0.12(Predicted)
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Safety

HS Code 
2933199090
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H317May cause an allergic skin reaction

H319Causes serious eye irritation

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.

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N-Bromosuccinimide Price

TRC
Product number
N498025
Product name
1-(3-Nitrophenyl)-1H-pyrazole
Packaging
5mg
Price
$45
Updated
2021/12/16
TRC
Product number
N498025
Product name
1-(3-Nitrophenyl)-1H-pyrazole
Packaging
50mg
Price
$90
Updated
2021/12/16
Apolloscientific
Product number
OR932686
Product name
1-(3-Nitrophenyl)-1H-pyrazole
Purity
95%
Packaging
250mg
Price
$189
Updated
2021/12/16
Apolloscientific
Product number
OR932686
Product name
1-(3-Nitrophenyl)-1H-pyrazole
Purity
95%
Packaging
1g
Price
$435
Updated
2021/12/16
Chemenu
Product number
CM187996
Product name
1-(3-nitrophenyl)-1H-pyrazole
Purity
95%
Packaging
1g
Price
$174
Updated
2021/12/16
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1-(3-nitrophenyl)-1H-pyrazole Chemical Properties,Usage,Production

Synthesis

288-13-1

645-00-1

25688-18-0

In a 50 mL round bottom flask, 1-iodo-3-nitrobenzene (1.0 mmol), pyrazole (1.2 mmol), ligand (0.04 mmol), cuprous oxide (0.10 mmol), cesium carbonate (2.0 mmol), and dry solvent (20 mL) were added sequentially. The reaction system was placed under nitrogen protection. The reaction mixture was heated to the indicated temperature in an oil bath under continuous stirring and cooled to room temperature after 20 h of reaction. The reaction mixture was filtered through a porous filter funnel filled with diatomaceous earth and the filter cake was washed with ethyl acetate. If DMSO is used as solvent, the filtrate is washed three times with 25 mL of water for extraction. The organic phases were combined, dried with anhydrous magnesium sulfate, and concentrated under reduced pressure to remove the solvent to give the crude product. Finally, the crude product was purified by silica gel column chromatography, and the eluent was a solvent mixture of hexane and ethyl acetate in a volume ratio of 3:1.

References

[1] Journal of Organic Chemistry, 2007, vol. 72, # 23, p. 8969 - 8971
[2] Tetrahedron Letters, 2016, vol. 57, # 20, p. 2197 - 2200
[3] Angewandte Chemie, International Edition, 2009, vol. 48, # 40, p. 7398 - 7401
[4] Angewandte Chemie, 2009, vol. 121, # 40, p. 7534 - 7537
[5] Tetrahedron Letters, 2011, vol. 52, # 52, p. 7171 - 7174

1-(3-nitrophenyl)-1H-pyrazole Preparation Products And Raw materials

Raw materials

Preparation Products

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25688-18-0, 1-(3-nitrophenyl)-1H-pyrazoleRelated Search:


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  • 25688-18-0