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
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
UNII
  • 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
  • CNCCC1=CNC2=CC=C(C=C21)OC
Properties
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 ?)

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.

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

See also

References

  1. ^ Wilkinson, S. (1958). "428. 5-Methoxy-N-methyltryptamine: a new indole alkaloid from Phalaris arundinacea L.". Journal of the Chemical Society (Resumed): 2079. doi:10.1039/jr9580002079.
  2. ^ 5-MeO-NMT Entry in TIHKAL


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