ChemicalBook--->CAS DataBase List--->367-80-6

367-80-6

367-80-6 Structure

367-80-6 Structure
IdentificationMore
[Name]

Ethyl 4-fluoro-3-nitrobenzoate
[CAS]

367-80-6
[Synonyms]

4-FLUORO-3-NITROBENZOIC ACID ETHYL ESTER
ETHYL 4-FLUORO-3-NITROBENZOATE
RARECHEM AL BI 0858
[Molecular Formula]

C9H8FNO4
[MDL Number]

MFCD03428515
[Molecular Weight]

213.16
[MOL File]

367-80-6.mol
Chemical PropertiesBack Directory
[Melting point ]

45.3 °C
[Boiling point ]

312.3±22.0 °C(Predicted)
[density ]

1.333±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[form ]

crystalline powder
[color ]

Pale creamy lemon
[CAS DataBase Reference]

367-80-6(CAS DataBase Reference)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[HS Code ]

2918300090
Spectrum DetailBack Directory
[Spectrum Detail]

Ethyl 4-fluoro-3-nitrobenzoate(367-80-6)1HNMR
Hazard InformationBack Directory
[Synthesis]

Ethanol

64-17-5

4-Fluoro-3-nitrobenzoic acid

453-71-4

Ethyl 4-fluoro-3-nitrobenzoate

367-80-6

Step 1: 5.00 g (27.0 mmol) of 4-fluoro-3-nitrobenzoic acid was dissolved in 50 mL of saturated ethanolic hydrochloric acid solution (1.25 M) and the reaction was refluxed for 15 hours. After completion of the reaction, the reaction mixture was evaporated using a rotary evaporator. Purification by fast column chromatography [silica gel, eluent petroleum ether/ethyl acetate (4:1)] afforded 5.48 g (25.7 mmol, 95%) of ethyl 4-fluoro-3-nitrobenzoate as a colorless solid. Thin layer chromatography (TLC) Rf = 0.48 [silica gel, petroleum ether/ethyl acetate (4:1)]. Mass Spectrometry (ESI) m/z: [M + H]+ calculated value of 214.

[References]

[1] Bioorganic and Medicinal Chemistry Letters, 2006, vol. 16, # 7, p. 1859 - 1863
[2] Patent: US2007/112033, 2007, A1. Location in patent: Page/Page column 17-18
[3] Patent: US2013/79306, 2013, A1. Location in patent: Paragraph 0226; 0227; 0228; 0229
[4] Journal of Medicinal Chemistry, 2012, vol. 55, # 16, p. 7262 - 7272
[5] Journal of Medicinal Chemistry, 2018, vol. 61, # 4, p. 1646 - 1663
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