Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C11H15NO |
| Molecular Weight | 177.2429 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(N)CC1=CC=C2OCCC2=C1
InChI
InChIKey=PZTJXZKNTPCPJL-UHFFFAOYSA-N
InChI=1S/C11H15NO/c1-8(12)6-9-2-3-11-10(7-9)4-5-13-11/h2-3,7-8H,4-6,12H2,1H3
Approval Year
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Preferred Name | English | ||
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Code | English | ||
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WIKIPEDIA |
Designer-drugs-5-APDB
Created by
admin on Mon Mar 31 21:38:11 GMT 2025 , Edited by admin on Mon Mar 31 21:38:11 GMT 2025
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| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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DTXSID70934560
Created by
admin on Mon Mar 31 21:38:11 GMT 2025 , Edited by admin on Mon Mar 31 21:38:11 GMT 2025
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PRIMARY | |||
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152624-03-8
Created by
admin on Mon Mar 31 21:38:11 GMT 2025 , Edited by admin on Mon Mar 31 21:38:11 GMT 2025
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PRIMARY | |||
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UI10BAJ8SH
Created by
admin on Mon Mar 31 21:38:11 GMT 2025 , Edited by admin on Mon Mar 31 21:38:11 GMT 2025
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PRIMARY | |||
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5-APDB
Created by
admin on Mon Mar 31 21:38:11 GMT 2025 , Edited by admin on Mon Mar 31 21:38:11 GMT 2025
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PRIMARY | 5-(2-Aminopropyl)-2,3-dihydrobenzofuran (5-APDB, 3-Desoxy-MDA, EMA-4) is a putative entactogen drug of the phenethylamine and amphetamine classes.[1] It is an analogue of MDA where the heterocyclic 3-position oxygen from the 3,4-methylenedioxy ring has been replaced by a methylene bridge.[1] 6-APDB is an analogue of 5-APDB where the 4-position oxygen has been replaced by a methylene bridge instead.[1] 5-APDB was developed by a team led by David E. Nichols at Purdue University as part of their research into non-neurotoxic analogues of MDMA.[1] | ||
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192601
Created by
admin on Mon Mar 31 21:38:11 GMT 2025 , Edited by admin on Mon Mar 31 21:38:11 GMT 2025
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PRIMARY |
ACTIVE MOIETY
