ChemicalBook--->CAS DataBase List--->4850-93-5

4850-93-5

4850-93-5 Structure

4850-93-5 Structure
IdentificationBack Directory
[Name]

N-(4-Nitrophenyl)propionamide
[CAS]

4850-93-5
[Synonyms]

N-(4-Nitrophenyl)
4-NITROPROPIONANILIDE
P-NITRO PROPIONANILIDE
3-NITRO PROPIONANILIDE
Nitro propionyl aniline
4-Nitro-propionylanilide
P-NITRO-PROPIONYLANILIDE
N-(4-NITROPHENYL)PROPIONAMIDE
Propanamide, N-(4-nitrophenyl)-
[Molecular Formula]

C9H10N2O3
[MDL Number]

MFCD00791260
[MOL File]

4850-93-5.mol
[Molecular Weight]

194.19
Chemical PropertiesBack Directory
[Melting point ]

182 °C
[Boiling point ]

411.7±28.0 °C(Predicted)
[density ]

1.287±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[pka]

13.91±0.70(Predicted)
Safety DataBack Directory
[HS Code ]

2924297099
Hazard InformationBack Directory
[Synthesis]

Propionyl chloride

79-03-8

4-Nitroaniline

100-01-6

N-(4-Nitrophenyl)propionamide

4850-93-5

General procedure for the synthesis of p-nitropropionanilide from propionyl chloride and 4-nitroanilide: To a solution of 4-nitroanilide (7.5 mmol, 1.04 g) in dichloromethane (30 mL) was slowly added propionyl chloride (7.5 mmol, 0.70 mL). The reaction mixture was stirred at room temperature overnight. Upon completion of the reaction, the mixture was filtered and the filtrate was concentrated under reduced pressure by rotary evaporator to remove the solvent. The crude product was washed with hexane (10 mL) to remove impurities. Finally, the product was dried under vacuum to afford the target compound N-(4-nitrophenyl)propionamide in white powder form in a yield of 0.38 g (26% yield).

[References]

[1] Dalton Transactions, 2014, vol. 43, # 23, p. 8888 - 8893
[2] Patent: US2014/228579, 2014, A1. Location in patent: Paragraph 0155
[3] Pest Management Science, 2000, vol. 56, # 7, p. 607 - 614
[4] Bioorganic and Medicinal Chemistry, 2008, vol. 16, # 23, p. 10034 - 10042
[5] Patent: WO2010/129053, 2010, A2. Location in patent: Page/Page column 112-113
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