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454-16-0

454-16-0 Structure

454-16-0 Structure
IdentificationBack Directory
[Name]

2-Fluoro-5-nitroanisole
[CAS]

454-16-0
[Synonyms]

454-16-0
2-Fluoro-5-nitroasinole
2-Fluoro-5-nitroanisole
3-Methoxy-4-fluoronitrobenzene
4-Fluoro-3-methoxynitrobenzene
Anisole, 2-fluoro-5-nitro- (8CI)
1-Fluoro-2-methoxy-4-nitrobenzene
Benzene, 1-fluoro-2-methoxy-4-nitro-
4-Fluoro-3-methoxynitrobenzene 2-Fluoro-5-nitroanisole
2-Fluoro-5-nitroanisole[4-Fluoro-3-Methoxynitrobenzene]
4-Fluoro-3-methoxynitrobenzene, 1-Fluoro-2-methoxy-4-nitrobenzene, 2-Fluoro-5-nitrophenyl methyl ether
[EINECS(EC#)]

688-393-0
[Molecular Formula]

C7H6FNO3
[MDL Number]

MFCD07782081
[MOL File]

454-16-0.mol
[Molecular Weight]

171.13
Chemical PropertiesBack Directory
[Melting point ]

69-71 °C
[Boiling point ]

270.3±20.0 °C(Predicted)
[density ]

1.321±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[solubility ]

Chloroform (Slightly), Methanol (Slightly)
[form ]

Solid
[color ]

Light Yellow to Yellow
[InChI]

InChI=1S/C7H6FNO3/c1-12-7-4-5(9(10)11)2-3-6(7)8/h2-4H,1H3
[InChIKey]

AZNKKZHZGDZSIF-UHFFFAOYSA-N
[SMILES]

C1(F)=CC=C([N+]([O-])=O)C=C1OC
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[Hazard Codes ]

Xi
[HS Code ]

2909309090
Spectrum DetailBack Directory
[Spectrum Detail]

2-Fluoro-5-nitroanisole(454-16-0)1HNMR
2-Fluoro-5-nitroanisole(454-16-0)19FNMR
Hazard InformationBack Directory
[Synthesis]

2-FLUORO-5-NITROPHENOL

22510-08-3

Iodomethane

74-88-4

2-Fluoro-5-nitroanisole

454-16-0

GENERAL STEPS: Potassium carbonate (K2CO3, 5.27 g, 38.1 mmol) was added to a solution of 2-fluoro-5-nitrophenol (5.0 g, 31.84 mmol) in N,N-dimethylformamide (DMF, 50 mL), and the mixture was stirred for 15 minutes at room temperature. Subsequently, iodomethane (3 mL, 47.7 mmol) was added and the reaction mixture continued to be stirred for 2 hours at room temperature. Upon completion of the reaction, the mixture was poured into ice water and the solid product was isolated by filtration. The solid was washed well with deionized water and subsequently dried under vacuum to afford the off-white solid product 2-fluoro-5-nitroanisole (4.0 g, 73.5% yield). The structure of the product was confirmed by 1H NMR (300 MHz, CDCl3): δ 7.89-7.84 (m, 2H), 7.25-7.17 (m, 1H), 3.98 (s, 3H).

[References]

[1] Patent: WO2015/104653, 2015, A1. Location in patent: Page/Page column 57
[2] Patent: US2016/368906, 2016, A1. Location in patent: Paragraph 0229
[3] Patent: US2014/57911, 2014, A1. Location in patent: Paragraph 0635
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