5-MeO-NMT

5-MeO-NMT

Names
Preferred IUPAC name 2-(5-Methoxy-1H-indol-3-yl)-N-methylethan-1-amine
Other names 5-Methoxy-N-methyltryptamine
Identifiers
CAS Number	2009-03-2 (freebase) Y 2426-68-8 (hydrochloride) Y
3D model (JSmol)	Interactive image
ChEBI	CHEBI:189635 Y
ChEMBL	ChEMBL58579 Y
ChemSpider	15360 Y
PubChem CID	16184
UNII	YBO217L5YV (freebase) Y 3390M5391J (hydrochloride) Y
CompTox Dashboard (EPA)	DTXSID40173909
InChI InChI=1S/C12H16N2O/c1-13-6-5-9-8-14-12-4-3-10(15-2)7-11(9)12/h3-4,7-8,13-14H,5-6H2,1-2H3 Y Key: NFDDCRIHMZGWBP-UHFFFAOYSA-N Y InChI=1/C12H16N2O/c1-13-6-5-9-8-14-12-4-3-10(15-2)7-11(9)12/h3-4,7-8,13-14H,5-6H2,1-2H3 Key: NFDDCRIHMZGWBP-UHFFFAOYAI
SMILES CNCCC1=CNC2=CC=C(C=C21)OC
Properties
Chemical formula	C12H16N2O
Molar mass	204.273 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). N verify (what is YN ?) Infobox references

5-MeO-NMT (5-methoxy-N-methyltryptamine) is an organic chemical compound, being the 5-methoxy analog of N-methyltryptamine (NMT). It was first isolated from Phalaris arundinacea (reed canary grass). It has also been synthesized by Alexander Shulgin and reported in his book TiHKAL.

Legal status

In the United States, this substance is a Schedule 1 isomer of Bufotenin.

See also

• Tryptamine
• Dimethyltryptamine
• Psychedelics, dissociatives and deliriants