Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C6H3F3 |
| Molecular Weight | 132.0832 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
FC1=CC=C(F)C(F)=C1
InChI
InChIKey=PEBWOGPSYUIOBP-UHFFFAOYSA-N
InChI=1S/C6H3F3/c7-4-1-2-5(8)6(9)3-4/h1-3H
| Molecular Formula | C6H3F3 |
| Molecular Weight | 132.0832 |
| 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 |
|---|---|---|
| The effects of volatile aromatic anesthetics on voltage-gated Na+ channels expressed in Xenopus oocytes. | 2008-11 |
|
| C-F activation of fluorinated arenes using NHC-stabilized nickel(0) complexes: selectivity and mechanistic investigations. | 2008-07-23 |
|
| A convenient catalyst system for microwave accelerated cross-coupling of a range of aryl boronic acids with aryl chlorides. | 2007-05-30 |
|
| Contrasting roles of the N-methyl-D-aspartate receptor in the production of immobilization by conventional and aromatic anesthetics. | 2006-05 |
|
| Photodissociation dynamics of C6HxF6-x (x = 1-4) at 193 nm. | 2005-05-05 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:39:55 GMT 2025
by
admin
on
Mon Mar 31 19:39:55 GMT 2025
|
| Record UNII |
QWW4HNQ0L1
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Preferred Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
QWW4HNQ0L1
Created by
admin on Mon Mar 31 19:39:55 GMT 2025 , Edited by admin on Mon Mar 31 19:39:55 GMT 2025
|
PRIMARY | |||
|
367-23-7
Created by
admin on Mon Mar 31 19:39:55 GMT 2025 , Edited by admin on Mon Mar 31 19:39:55 GMT 2025
|
PRIMARY | |||
|
DTXSID30190140
Created by
admin on Mon Mar 31 19:39:55 GMT 2025 , Edited by admin on Mon Mar 31 19:39:55 GMT 2025
|
PRIMARY | |||
|
206-684-9
Created by
admin on Mon Mar 31 19:39:55 GMT 2025 , Edited by admin on Mon Mar 31 19:39:55 GMT 2025
|
PRIMARY | |||
|
10263
Created by
admin on Mon Mar 31 19:39:55 GMT 2025 , Edited by admin on Mon Mar 31 19:39:55 GMT 2025
|
PRIMARY | |||
|
67773
Created by
admin on Mon Mar 31 19:39:55 GMT 2025 , Edited by admin on Mon Mar 31 19:39:55 GMT 2025
|
PRIMARY |