Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C20H21N |
| Molecular Weight | 275.3874 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 1 |
| Charge | 0 |
| Stereo Comments | Assumed racemic |
SHOW SMILES / InChI
SMILES
CNCC\C=C1\C2=CC=CC=C2[C@H]3C[C@H]3C4=CC=CC=C14
InChI
InChIKey=MILRTYCRJIRPKY-IKXRLOQMSA-N
InChI=1S/C20H21N/c1-21-12-6-11-16-14-7-2-4-9-17(14)19-13-20(19)18-10-5-3-8-15(16)18/h2-5,7-11,19-21H,6,12-13H2,1H3/b16-11-/t19-,20+/m1/s1
Approval Year
| Name | Type | Language | ||
|---|---|---|---|---|
|
Preferred Name | English | ||
|
Official Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
C174650
Created by
admin on Mon Mar 31 18:15:04 GMT 2025 , Edited by admin on Mon Mar 31 18:15:04 GMT 2025
|
PRIMARY | |||
|
3728
Created by
admin on Mon Mar 31 18:15:04 GMT 2025 , Edited by admin on Mon Mar 31 18:15:04 GMT 2025
|
PRIMARY | |||
|
C3X0UOC25D
Created by
admin on Mon Mar 31 18:15:04 GMT 2025 , Edited by admin on Mon Mar 31 18:15:04 GMT 2025
|
PRIMARY | |||
|
CHEMBL2110951
Created by
admin on Mon Mar 31 18:15:04 GMT 2025 , Edited by admin on Mon Mar 31 18:15:04 GMT 2025
|
PRIMARY | |||
|
DTXSID10963758
Created by
admin on Mon Mar 31 18:15:04 GMT 2025 , Edited by admin on Mon Mar 31 18:15:04 GMT 2025
|
PRIMARY | |||
|
47166-67-6
Created by
admin on Mon Mar 31 18:15:04 GMT 2025 , Edited by admin on Mon Mar 31 18:15:04 GMT 2025
|
PRIMARY | |||
|
100000083289
Created by
admin on Mon Mar 31 18:15:04 GMT 2025 , Edited by admin on Mon Mar 31 18:15:04 GMT 2025
|
PRIMARY | |||
|
Octriptyline
Created by
admin on Mon Mar 31 18:15:04 GMT 2025 , Edited by admin on Mon Mar 31 18:15:04 GMT 2025
|
PRIMARY | |||
|
SUB09418MIG
Created by
admin on Mon Mar 31 18:15:04 GMT 2025 , Edited by admin on Mon Mar 31 18:15:04 GMT 2025
|
PRIMARY |
ACTIVE MOIETY
SALT/SOLVATE (PARENT)