DALT

DALT
Clinical data
Routes of; administration	Oral, insufflated, rectal, smoked, IM, IV[citation needed]
ATC code	none
Legal status
Legal status	May be covered under the Federal Analog Act in the United States and under similar bills in other countries;
Identifiers
	IUPAC name N-Allyl-N-[2-(1H-indol-3-yl)ethyl]prop-2-en-1-amine;
PubChem (CID)	24839550
ChemSpider	21250454
Chemical and physical data
Formula	C16H20N2
Molar mass	240.34 g/mol
3D model (Jmol)	Interactive image
	SMILES C=CCN(CC=C)CCc2cnc1ccccc12 ;
	InChI InChI=1S/C16H20N2/c1-3-10-18(11-4-2)12-9-14-13-17-16-8-6-5-7-15(14)16/h3-8,13,17H,1-2,9-12H2 ; Key:LQEATNFJCMVKAC-UHFFFAOYSA-N ;
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N,N-Diallyltryptamine (DALT) is a tryptamine derivative. It has been used as an intermediate in the preparation of radiolabeled diethyltryptamine.^[1]

References[edit]

^ Brandt, SD; Tirunarayanapuram, SS; Freeman, S; Dempster, N; Barker, SA; Daley, PF; Cozzi, NV; Martins, CPB (2008). "Microwave-accelerated synthesis of psychoactive deuterated N,N-dialkylated-[α,α,β,β-d4]-tryptamines". J. Labelled Compd. Radiopharm. 51 (14): 423–429. doi:10.1002/jlcr.1557.

Clinical data

Routes of administration	Oral, insufflated, rectal, smoked, IM, IV^{[citation needed]}
ATC code	none
Legal status
Legal status	May be covered under the Federal Analog Act in the United States and under similar bills in other countries
Identifiers
IUPAC name N-Allyl-N-[2-(1H-indol-3-yl)ethyl]prop-2-en-1-amine
PubChem (CID)	24839550
ChemSpider	21250454^Y
Chemical and physical data
Formula	C₁₆H₂₀N₂
Molar mass	240.34 g/mol
3D model (Jmol)	Interactive image
SMILES C=CCN(CC=C)CCc2cnc1ccccc12
InChI InChI=1S/C16H20N2/c1-3-10-18(11-4-2)12-9-14-13-17-16-8-6-5-7-15(14)16/h3-8,13,17H,1-2,9-12H2^Y Key:LQEATNFJCMVKAC-UHFFFAOYSA-N^Y
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