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Details

Stereochemistry ACHIRAL
Molecular Formula C6H6FN
Molecular Weight 111.1169
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 4-Fluoroaniline

SMILES

NC1=CC=C(F)C=C1

InChI

InChIKey=KRZCOLNOCZKSDF-UHFFFAOYSA-N
InChI=1S/C6H6FN/c7-5-1-3-6(8)4-2-5/h1-4H,8H2

HIDE SMILES / InChI

Molecular Formula C6H6FN
Molecular Weight 111.1169
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Dichlorido(η-p-cymene)(4-fluoro-aniline-κN)ruthenium(II).
2010-12-18
4-(4-Fluoro-anilino)-N-(4-fluoro-phen-yl)-3-nitro-benzamide.
2010-10-23
N-[(2-Chloro-3-quinol-yl)meth-yl]-4-fluoro-aniline.
2010-09-11
4,5,6,7-Tetra-chloro-2-(4-fluoro-phen-yl)isoindoline-1,3-dione.
2010-06-23
4-Fluoro-anilinium tetra-chloridoferrate(III) 18-crown-6 clathrate.
2010-06-05
Formation of a quinoneimine intermediate of 4-fluoro-N-methylaniline by FMO1: carbon oxidation plus defluorination.
2010-05-17
Investigating the mechanisms of aromatic amine-induced protein free radical formation by quantitative structure-activity relationships: implications for drug-induced agranulocytosis.
2010-05-17
Bis(4-fluoro-anilinium) tetra-chloridocuprate(II).
2010-05-15
Synthesis and Pharmacological Evaluation of Novel Schiff Base Analogues of 3-(4-amino) Phenylimino) 5-fluoroindolin-2-one.
2010-04
6-Fluoro-1,3,4-triphenyl-1H-pyrazolo[3,4-b]quinoline benzene hemisolvate.
2010-02-10
N-(2-Fluoro-phen-yl)cinnamamide.
2010-02-06
(E)-2-[(4-Fluoro-phen-yl)imino-meth-yl]-5-methoxy-phenol.
2010-01-09
3,6-Dichloro-N-(4-fluoro-phen-yl)picolinamide.
2009-07-04
Phenyl N-(4-fluorophen-yl)carbamate.
2009-04-18
(E)-Ethyl 3-(4-fluoro-anilino)-2-(4-methoxy-phen-yl)acrylate.
2008-11-26
2-Bromo-4-chloro-6-(4-fluoro-phenyl-imino-meth-yl)phenol.
2008-06-25
Theoretical Raman and infrared spectra, and vibrational assignment for para-halogenoanilines: DFT study.
2007-11
Synthesis and antitumor activity of some novel quinazoline derivatives bearing the biologically active thione moiety.
2006
N-acylanilines, herbicide-CHA chimera, and amino acid analogues as novel chemical hybridizing agents for wheat (Triticum aestivum L.).
2005-10-05
Convenient access both to highly antimalaria-active 10-arylaminoartemisinins, and to 10-alkyl ethers including artemether, arteether, and artelinate.
2005-04
Schiff bases of gossypol: an NMR and DFT study.
2005-04
Hydrogen bonding in 1:1 proton-transfer compounds of 5-sulfosalicylic acid with 4-X-substituted anilines (X = F, Cl or Br).
2005-02
Potential of neurotoxicity after a single oral dose of 4-bromo-, 4-chloro-, 4-fluoro- or 4-iodoaniline in rats.
2003-09-17
Metabolism of 4-fluoroaniline and 4-fluorobiphenyl in the earthworm Eisenia veneta characterized by high-resolution NMR spectroscopy with directly coupled HPLC-NMR and HPLC-MS.
2002-06
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:36:55 GMT 2025
Edited
by admin
on Mon Mar 31 19:36:55 GMT 2025
Record UNII
60HI1G076Z
Record Status Validated (UNII)
Record Version
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Name Type Language
4-Fluoroaniline
HSDB   MI  
Common Name English
NSC-579
Preferred Name English
Aniline, p-fluoro-
Common Name English
4-Fluoroaniline [HSDB]
Common Name English
4-Fluorobenzenamine
Systematic Name English
4-Fluoro-1-benzenamine
Systematic Name English
Fluoroaniline, P-
Common Name English
1-Amino-4-fluorobenzene
Systematic Name English
4-Fluoroaniline [MI]
Common Name English
Code System Code Type Description
CHEBI
28546
Created by admin on Mon Mar 31 19:36:55 GMT 2025 , Edited by admin on Mon Mar 31 19:36:55 GMT 2025
PRIMARY
MERCK INDEX
m5470
Created by admin on Mon Mar 31 19:36:55 GMT 2025 , Edited by admin on Mon Mar 31 19:36:55 GMT 2025
PRIMARY Merck Index
NSC
579
Created by admin on Mon Mar 31 19:36:55 GMT 2025 , Edited by admin on Mon Mar 31 19:36:55 GMT 2025
PRIMARY
HSDB
2691
Created by admin on Mon Mar 31 19:36:55 GMT 2025 , Edited by admin on Mon Mar 31 19:36:55 GMT 2025
PRIMARY
CAS
371-40-4
Created by admin on Mon Mar 31 19:36:55 GMT 2025 , Edited by admin on Mon Mar 31 19:36:55 GMT 2025
PRIMARY
ECHA (EC/EINECS)
206-735-5
Created by admin on Mon Mar 31 19:36:55 GMT 2025 , Edited by admin on Mon Mar 31 19:36:55 GMT 2025
PRIMARY
EPA CompTox
DTXSID9022027
Created by admin on Mon Mar 31 19:36:55 GMT 2025 , Edited by admin on Mon Mar 31 19:36:55 GMT 2025
PRIMARY
MESH
C043455
Created by admin on Mon Mar 31 19:36:55 GMT 2025 , Edited by admin on Mon Mar 31 19:36:55 GMT 2025
PRIMARY
FDA UNII
60HI1G076Z
Created by admin on Mon Mar 31 19:36:55 GMT 2025 , Edited by admin on Mon Mar 31 19:36:55 GMT 2025
PRIMARY
PUBCHEM
9731
Created by admin on Mon Mar 31 19:36:55 GMT 2025 , Edited by admin on Mon Mar 31 19:36:55 GMT 2025
PRIMARY