4-Fluoronitrobenzene

4-Fluoronitrobenzene

Names
Preferred IUPAC name 1-Fluoro-4-nitrobenzene
Other names 1-nitro-4-fluorobenzene
Identifiers
CAS Number	350-46-9 Y
3D model (JSmol)	Interactive image
ChEMBL	ChEMBL163729
ChemSpider	13856885
ECHA InfoCard	100.005.912
EC Number	206-502-8
PubChem CID	9590
UNII	A2M2FH7XHH
CompTox Dashboard (EPA)	DTXSID9022025
InChI InChI=1S/C6H4FNO2/c7-5-1-3-6(4-2-5)8(9)10/h1-4H Key: WFQDTOYDVUWQMS-UHFFFAOYSA-N
SMILES C1=CC(=CC=C1[N+](=O)[O-])F
Properties
Chemical formula	C6H4FNO2
Molar mass	141.101 g·mol−1
Appearance	yellow solid, melting near room temperature
Density	1.340 g/cm3
Melting point	22–24 °C (72–75 °F; 295–297 K)
Boiling point	206 °C (403 °F; 479 K)
Hazards
GHS labelling:[1]
Pictograms
Signal word	Danger
Hazard statements	H301, H302, H312, H317, H331, H373, H412
Precautionary statements	P260, P264, P270, P271, P272, P273, P280, P301+P316, P301+P317, P302+P352, P304+P340, P316, P317, P319, P321, P330, P333+P313, P362+P364, P403+P233, P405, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

4-Fluoronitrobenzene is an organic compound with the formula FC₆H₄NO₂. It is one of three isomeric fluoronitrobenzenes.^[2] A yellow oil, it is prepared from 4-nitrochlorobenzene using the Halex process:

O₂NC₆H₄Cl + KF → O₂NC₆H₄F + KCl

4-Fluoronitrobenzene can be hydrogenated to give 4-fluoroaniline,^[3] which is a precursor to the fungicide fluoroimide [de] and parafluorofentanyl.

Owing to the presence of the electron withdrawing nitro group, the fluoride is a good leaving group in fluoronitrobenzenes. Thus reaction with phenoxide gives the mononitrodiphenylether.^[4]