Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C22H28N2O |
| Molecular Weight | 336.4705 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCC(=O)N([C@@H]1CCN(CC2=CC=CC=C2)C[C@@H]1C)C3=CC=CC=C3
InChI
InChIKey=MSAFCEWTMBDBFQ-GHTZIAJQSA-N
InChI=1S/C22H28N2O/c1-3-22(25)24(20-12-8-5-9-13-20)21-14-15-23(16-18(21)2)17-19-10-6-4-7-11-19/h4-13,18,21H,3,14-17H2,1-2H3/t18-,21+/m0/s1
Approval Year
| Name | Type | Language | ||
|---|---|---|---|---|
|
Preferred Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
|
CDC |
(±)-cis-Isofentanyl
Created by
admin on Wed Apr 02 05:45:28 GMT 2025 , Edited by admin on Wed Apr 02 05:45:28 GMT 2025
|
||
|
WIKIPEDIA |
List_of_fentanyl_analogues
Created by
admin on Wed Apr 02 05:45:28 GMT 2025 , Edited by admin on Wed Apr 02 05:45:28 GMT 2025
|
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
71313860
Created by
admin on Wed Apr 02 05:45:28 GMT 2025 , Edited by admin on Wed Apr 02 05:45:28 GMT 2025
|
PRIMARY | |||
|
BT57ARH9QX
Created by
admin on Wed Apr 02 05:45:28 GMT 2025 , Edited by admin on Wed Apr 02 05:45:28 GMT 2025
|
PRIMARY | |||
|
42045-84-1
Created by
admin on Wed Apr 02 05:45:28 GMT 2025 , Edited by admin on Wed Apr 02 05:45:28 GMT 2025
|
NON-SPECIFIC STEREOCHEMISTRY | |||
|
DTXSID00747120
Created by
admin on Wed Apr 02 05:45:28 GMT 2025 , Edited by admin on Wed Apr 02 05:45:28 GMT 2025
|
PRIMARY | |||
|
Isofentanyl
Created by
admin on Wed Apr 02 05:45:28 GMT 2025 , Edited by admin on Wed Apr 02 05:45:28 GMT 2025
|
PRIMARY | |||
|
79278-40-3
Created by
admin on Wed Apr 02 05:45:28 GMT 2025 , Edited by admin on Wed Apr 02 05:45:28 GMT 2025
|
PRIMARY |
ACTIVE MOIETY
SALT/SOLVATE (PARENT)
