Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C2HBrF4 |
| Molecular Weight | 180.927 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
FC(Br)C(F)(F)F
InChI
InChIKey=RZXZIZDRFQFCTA-UHFFFAOYSA-N
InChI=1S/C2HBrF4/c3-1(4)2(5,6)7/h1H
| Molecular Formula | C2HBrF4 |
| Molecular Weight | 180.927 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
Teflurane was first used in man in 1960. A series of thirty anesthetics completed in the first six months suggested that the teflurane was essentially non-toxic to the circulatory system and to hepatic and renal function. However, when the drug was given at inspired concentrations of 10 % and above, cardiac arrhythmias appeared, increased in severity and significance and systolic and diastolic blood pressures fell in direct proportion to the concentration given. That is why the further development of the teflurane was terminated.
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/4892959
Unknown
Route of Administration:
Other
| Substance Class |
Chemical
Created
by
admin
on
Edited
Wed Apr 02 08:21:12 GMT 2025
by
admin
on
Wed Apr 02 08:21:12 GMT 2025
|
| Record UNII |
6492U1O9V8
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Official Name | English | ||
|
Preferred Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Common Name | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
|
NCI_THESAURUS |
C245
Created by
admin on Wed Apr 02 08:21:12 GMT 2025 , Edited by admin on Wed Apr 02 08:21:12 GMT 2025
|
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
SUB10868MIG
Created by
admin on Wed Apr 02 08:21:12 GMT 2025 , Edited by admin on Wed Apr 02 08:21:12 GMT 2025
|
PRIMARY | |||
|
C152540
Created by
admin on Wed Apr 02 08:21:12 GMT 2025 , Edited by admin on Wed Apr 02 08:21:12 GMT 2025
|
PRIMARY | |||
|
1114
Created by
admin on Wed Apr 02 08:21:12 GMT 2025 , Edited by admin on Wed Apr 02 08:21:12 GMT 2025
|
PRIMARY | |||
|
124-72-1
Created by
admin on Wed Apr 02 08:21:12 GMT 2025 , Edited by admin on Wed Apr 02 08:21:12 GMT 2025
|
PRIMARY | |||
|
6492U1O9V8
Created by
admin on Wed Apr 02 08:21:12 GMT 2025 , Edited by admin on Wed Apr 02 08:21:12 GMT 2025
|
PRIMARY | |||
|
100000082440
Created by
admin on Wed Apr 02 08:21:12 GMT 2025 , Edited by admin on Wed Apr 02 08:21:12 GMT 2025
|
PRIMARY | |||
|
C005786
Created by
admin on Wed Apr 02 08:21:12 GMT 2025 , Edited by admin on Wed Apr 02 08:21:12 GMT 2025
|
PRIMARY | |||
|
Teflurane
Created by
admin on Wed Apr 02 08:21:12 GMT 2025 , Edited by admin on Wed Apr 02 08:21:12 GMT 2025
|
PRIMARY | |||
|
31300
Created by
admin on Wed Apr 02 08:21:12 GMT 2025 , Edited by admin on Wed Apr 02 08:21:12 GMT 2025
|
PRIMARY | |||
|
DTXSID10861765
Created by
admin on Wed Apr 02 08:21:12 GMT 2025 , Edited by admin on Wed Apr 02 08:21:12 GMT 2025
|
PRIMARY | |||
|
CHEMBL143941
Created by
admin on Wed Apr 02 08:21:12 GMT 2025 , Edited by admin on Wed Apr 02 08:21:12 GMT 2025
|
PRIMARY | |||
|
3583
Created by
admin on Wed Apr 02 08:21:12 GMT 2025 , Edited by admin on Wed Apr 02 08:21:12 GMT 2025
|
PRIMARY | |||
|
m10520
Created by
admin on Wed Apr 02 08:21:12 GMT 2025 , Edited by admin on Wed Apr 02 08:21:12 GMT 2025
|
PRIMARY | Merck Index |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
ACTIVE MOIETY |