Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C6H4FNO2 |
| Molecular Weight | 141.0999 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
[O-][N+](=O)C1=CC=C(F)C=C1
InChI
InChIKey=WFQDTOYDVUWQMS-UHFFFAOYSA-N
InChI=1S/C6H4FNO2/c7-5-1-3-6(4-2-5)8(9)10/h1-4H
| Molecular Formula | C6H4FNO2 |
| Molecular Weight | 141.0999 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| 4-(1,2,4-Triazol-1-yl)aniline. | 2010-12-18 |
|
| Experimental and computational thermodynamic study of three monofluoronitrobenzene isomers. | 2010-06-17 |
|
| N-[4-(4-Nitro-phen-oxy)phen-yl]propionamide. | 2008-10-25 |
|
| Molecular structure, conformation, and potential to internal rotation of 2,6- and 3,5-difluoronitrobenzene studied by gas-phase electron diffraction and quantum chemical calculations. | 2008-06-05 |
|
| 1,4-Bis(4-amino-phen-oxy)benzene. | 2008-02-13 |
|
| N-(n-Dec-yl)-4-nitro-aniline. | 2008-02-06 |
|
| Quantitative analysis of valienamine in the microbial degradation of validamycin A after derivatization with p-nitrofluorobenzene by reversed-phase high-performance liquid chromatography. | 2005-09-25 |
|
| Unprecedented chemistry of an aryloxychlorodiazirine: generation of a dihalodiazirine and diazirinone. | 2005-03-02 |
|
| Solvent effects and mechanism for a nucleophilic aromatic substitution from QM/MM simulations. | 2004-08-19 |
|
| Meisenheimer complexes bonded at carbon and at oxygen. | 2004-07 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 22:23:19 GMT 2025
by
admin
on
Mon Mar 31 22:23:19 GMT 2025
|
| Record UNII |
A2M2FH7XHH
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Systematic Name | English | ||
|
Preferred Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Code | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
350-46-9
Created by
admin on Mon Mar 31 22:23:19 GMT 2025 , Edited by admin on Mon Mar 31 22:23:19 GMT 2025
|
PRIMARY | |||
|
A2M2FH7XHH
Created by
admin on Mon Mar 31 22:23:19 GMT 2025 , Edited by admin on Mon Mar 31 22:23:19 GMT 2025
|
PRIMARY | |||
|
DTXSID9022025
Created by
admin on Mon Mar 31 22:23:19 GMT 2025 , Edited by admin on Mon Mar 31 22:23:19 GMT 2025
|
PRIMARY | |||
|
9590
Created by
admin on Mon Mar 31 22:23:19 GMT 2025 , Edited by admin on Mon Mar 31 22:23:19 GMT 2025
|
PRIMARY | |||
|
206-502-8
Created by
admin on Mon Mar 31 22:23:19 GMT 2025 , Edited by admin on Mon Mar 31 22:23:19 GMT 2025
|
PRIMARY | |||
|
10281
Created by
admin on Mon Mar 31 22:23:19 GMT 2025 , Edited by admin on Mon Mar 31 22:23:19 GMT 2025
|
PRIMARY | |||
|
2735
Created by
admin on Mon Mar 31 22:23:19 GMT 2025 , Edited by admin on Mon Mar 31 22:23:19 GMT 2025
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
PARENT -> IMPURITY |
|