6-APDB

6-APDB
Clinical data
Routes of; administration	By mouth
Drug class	Empathogen–entactogen; Stimulant
ATC code	None;
Legal status
Legal status	CA: Schedule I; DE: NpSG (Industrial and scientific use only); UK: Class B;
Identifiers
	IUPAC name 1-(2,3-dihydro-1-benzofuran-6-yl)propan-2-amine;
CAS Number	152623-93-3 ;
PubChem CID	192599;
ChemSpider	167141 ;
UNII	O72F3CP4O8;
ChEMBL	ChEMBL124055 ;
CompTox Dashboard (EPA)	DTXSID60934559 ;
Chemical and physical data
Formula	C11H15NO
Molar mass	177.247 g·mol−1
3D model (JSmol)	Interactive image;
	SMILES O2c1cc(ccc1CC2)CC(N)C;
	InChI InChI=1S/C11H15NO/c1-8(12)6-9-2-3-10-4-5-13-11(10)7-9/h2-3,7-8H,4-6,12H2,1H3 ; Key:VRNGXHJGMCJRSQ-UHFFFAOYSA-N ;
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6-(2-Aminopropyl)-2,3-dihydrobenzofuran (6-APDB, 4-Desoxy-MDA, EMA-3) is a stimulant and entactogen drug of the phenethylamine and amphetamine classes. It is an analogue of MDA where the heterocyclic 4-position oxygen from the 3,4-methylenedioxy ring has been replaced with a methylene bridge. 5-APDB (3-Desoxy-MDA) is an analogue of 6-APDB where the 3-position oxygen has been replaced with a methylene instead. 6-APDB, along with 5-APDB, was first synthesized by David E. Nichols in the early 1990s while investigating non-neurotoxic MDMA analogues.

Clinical data


Routes of administration	By mouth
Drug class	Empathogen–entactogen; Stimulant
ATC code	None
Legal status
Legal status	CA: Schedule I DE: NpSG (Industrial and scientific use only) UK: Class B
Identifiers
IUPAC name 1-(2,3-dihydro-1-benzofuran-6-yl)propan-2-amine
CAS Number	152623-93-3^N
PubChem CID	192599
ChemSpider	167141^Y
UNII	O72F3CP4O8
ChEMBL	ChEMBL124055^Y
CompTox Dashboard (EPA)	DTXSID60934559
Chemical and physical data
Formula	C₁₁H₁₅NO
Molar mass	177.247 g·mol⁻¹
3D model (JSmol)	Interactive image
SMILES O2c1cc(ccc1CC2)CC(N)C
InChI InChI=1S/C11H15NO/c1-8(12)6-9-2-3-10-4-5-13-11(10)7-9/h2-3,7-8H,4-6,12H2,1H3^Y Key:VRNGXHJGMCJRSQ-UHFFFAOYSA-N^Y
^NY (what is this?) (verify)