Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C27H34N2O3 |
| Molecular Weight | 434.5705 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COC(=O)C(NC(=O)C1=CC2=C(C=C1)N(CC3CCCCC3)C4=CC=CC=C24)C(C)(C)C
InChI
InChIKey=FAWVRKNYDPKTDZ-UHFFFAOYSA-N
InChI=1S/C27H34N2O3/c1-27(2,3)24(26(31)32-4)28-25(30)19-14-15-23-21(16-19)20-12-8-9-13-22(20)29(23)17-18-10-6-5-7-11-18/h8-9,12-16,18,24H,5-7,10-11,17H2,1-4H3,(H,28,30)
| Molecular Formula | C27H34N2O3 |
| Molecular Weight | 434.5705 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 23:21:53 GMT 2025
by
admin
on
Mon Mar 31 23:21:53 GMT 2025
|
| Record UNII |
806TLE17XB
|
| Record Status |
Validated (UNII)
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| Record Version |
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-
Download
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Preferred Name | English | ||
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Common Name | English |
| Code System | Code | Type | Description | ||
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MDMB-CHMCZCA
Created by
admin on Mon Mar 31 23:21:53 GMT 2025 , Edited by admin on Mon Mar 31 23:21:53 GMT 2025
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PRIMARY | |||
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139032947
Created by
admin on Mon Mar 31 23:21:53 GMT 2025 , Edited by admin on Mon Mar 31 23:21:53 GMT 2025
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PRIMARY | |||
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806TLE17XB
Created by
admin on Mon Mar 31 23:21:53 GMT 2025 , Edited by admin on Mon Mar 31 23:21:53 GMT 2025
|
PRIMARY | |||
|
MDMB-CHMCZCA
Created by
admin on Mon Mar 31 23:21:53 GMT 2025 , Edited by admin on Mon Mar 31 23:21:53 GMT 2025
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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ENANTIOMER -> RACEMATE |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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ACTIVE MOIETY |