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).^[1] It has also been synthesized by Alexander Shulgin and reported in his book TiHKAL.^[2] Like other members of the N-methyltryptamine family of compounds, 5-MeO-NMT is believed to produce few or no psychedelic effects, although very little data exists about its pharmacological properties or toxicity.

Legal Status[edit]

In the U.S. this substance is a schedule 1 isomer of Bufotenin.

See also[edit]

• Tryptamine
• Dimethyltryptamine
• Psychedelics, dissociatives and deliriants

References[edit]