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DMMDA-2

From Wikipedia, the free encyclopedia
Bioactive phenylethylamine
DMMDA-2
Names
Preferred IUPAC name
1-(6,7-Dimethoxy-2H-1,3-benzodioxol-5-yl)propan-2-amine
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
UNII
  • InChI=1S/C12H17NO4/c1-7(13)4-8-5-9-11(17-6-16-9)12(15-3)10(8)14-2/h5,7H,4,6,13H2,1-3H3 checkY
    Key: UQXNREZPUUGSKM-UHFFFAOYSA-N checkY
  • InChI=1/C12H17NO4/c1-7(13)4-8-5-9-11(17-6-16-9)12(15-3)10(8)14-2/h5,7H,4,6,13H2,1-3H3
    Key: UQXNREZPUUGSKM-UHFFFAOYAC
  • CC(N)Cc1cc2OCOc2c(OC)c1OC
Properties
C12H17NO4
Molar mass239.27 g/mol
Melting point178 to 180 °C (352 to 356 °F; 451 to 453 K)
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)
Chemical compound

DMMDA-2 is abioactivephenethylamine discussed byAlexander Shulgin in his bookPiHKAL (Phenethylamines i Have Known And Loved); however, he was not the first to synthesize it.[1] Shulgin comments in his book that a 50 milligram dose of DMMDA-2 produces similar effects to3,4-methylenedioxy-1-α-methylphenylethylamine.[1] DMMDA-2 can be synthesized fromdillapiole.[1]

DMMDA-2 is equivalent to 5 mescaline units. DMMDA-2's isomer DMMDA is equivalent to 12 mescaline units.[2]

References

[edit]
  1. ^abc"#59 DMMDA-2".PiHKAL: a chemical love story. Erowid. Retrieved22 November 2011.
  2. ^Clare, Brian W. (1990)."Structure-Activity Correlations for Psychotomimetics. 1. Phenylalkylamines: Electronic, Volume, and Hydrophobicity Parameters"(PDF).Journal of Medicinal Chemistry.33 (7):687–702. Retrieved2025-01-07.

Further reading

[edit]
Phenethylamines
Amphetamines
Phentermines
Cathinones
Phenylisobutylamines
Phenylalkylpyrrolidines
Catecholamines
(and close relatives)
Miscellaneous
Retrieved from "https://en.wikipedia.org/w/index.php?title=DMMDA-2&oldid=1269130198"
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