Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C29H38N2O4.2ClH |
| Molecular Weight | 551.545 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.Cl.[H][C@@]12CC(C[C@@H]3NCCC4=CC(OC)=C(OC)C=C34)=C(CC)CN1CCC5=CC(OC)=C(OC)C=C25
InChI
InChIKey=WNJZDNXVVDNPSI-LXTBHBSOSA-N
InChI=1S/C29H38N2O4.2ClH/c1-6-18-17-31-10-8-20-14-27(33-3)29(35-5)16-23(20)25(31)12-21(18)11-24-22-15-28(34-4)26(32-2)13-19(22)7-9-30-24;;/h13-16,24-25,30H,6-12,17H2,1-5H3;2*1H/t24-,25-;;/m0../s1
| 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 |
| Molecular Formula | C29H38N2O4 |
| Molecular Weight | 478.623 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 05:50:22 UTC 2023
by
admin
on
Sat Dec 16 05:50:22 UTC 2023
|
| Record UNII |
3DU466HR53
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
71587420
Created by
admin on Sat Dec 16 05:50:22 UTC 2023 , Edited by admin on Sat Dec 16 05:50:22 UTC 2023
|
PRIMARY | |||
|
3DU466HR53
Created by
admin on Sat Dec 16 05:50:22 UTC 2023 , Edited by admin on Sat Dec 16 05:50:22 UTC 2023
|
PRIMARY | |||
|
112001-55-5
Created by
admin on Sat Dec 16 05:50:22 UTC 2023 , Edited by admin on Sat Dec 16 05:50:22 UTC 2023
|
PRIMARY | |||
|
DTXSID50149817
Created by
admin on Sat Dec 16 05:50:22 UTC 2023 , Edited by admin on Sat Dec 16 05:50:22 UTC 2023
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
ACTIVE MOIETY |