Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C24H30N2O.ClH |
| Molecular Weight | 398.969 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.O=C(C1CCC1)N(C2CCN(CCC3=CC=CC=C3)CC2)C4=CC=CC=C4
InChI
InChIKey=UMBMPZKCTUJNNA-UHFFFAOYSA-N
InChI=1S/C24H30N2O.ClH/c27-24(21-10-7-11-21)26(22-12-5-2-6-13-22)23-15-18-25(19-16-23)17-14-20-8-3-1-4-9-20;/h1-6,8-9,12-13,21,23H,7,10-11,14-19H2;1H
| Molecular Formula | C24H30N2O |
| Molecular Weight | 362.5078 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
| Molecular Formula | ClH |
| Molecular Weight | 36.461 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 19:00:39 GMT 2023
by
admin
on
Sat Dec 16 19:00:39 GMT 2023
|
| Record UNII |
QYC4B7S9AX
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
2306827-56-3
Created by
admin on Sat Dec 16 19:00:39 GMT 2023 , Edited by admin on Sat Dec 16 19:00:39 GMT 2023
|
PRIMARY | |||
|
QYC4B7S9AX
Created by
admin on Sat Dec 16 19:00:39 GMT 2023 , Edited by admin on Sat Dec 16 19:00:39 GMT 2023
|
PRIMARY | |||
|
DTXSID401036800
Created by
admin on Sat Dec 16 19:00:39 GMT 2023 , Edited by admin on Sat Dec 16 19:00:39 GMT 2023
|
PRIMARY | |||
|
139597318
Created by
admin on Sat Dec 16 19:00:39 GMT 2023 , Edited by admin on Sat Dec 16 19:00:39 GMT 2023
|
PRIMARY | PUBCHEM |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
PARENT -> SALT/SOLVATE |
|
