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DOM-2,5-DiEtO

From Wikipedia, the free encyclopedia

DOM-2,5-DiEtO
Clinical data
Other namesDOM-DiEtO; DOM-Di-EtO; DOM-DIETO; DOM-DI-ETO; 2,5-Diethoxy-4-methylamphetamine; 4-Methyl-2,5-diethoxyamphetamine
Routes of
administration
Unknown[1][2]
Drug classPossible stimulant[1][2]
ATC code
  • None
Pharmacokinetic data
Duration of actionUnknown[1][2]
Identifiers
  • 1-(2,5-diethoxy-4-methylphenyl)propan-2-amine
Chemical and physical data
3D model (JSmol)
  • CCOC1=CC(CC(N)C)=C(OCC)C=C1C
  • InChI=1S/C14H23NO2/c1-5-16-13-9-12(8-11(4)15)14(17-6-2)7-10(13)3/h7,9,11H,5-6,8,15H2,1-4H3
  • Key:IFOVMAYZCWAFKA-UHFFFAOYSA-N

DOM-2,5-DiEtO, also known as 2,5-diethoxy-4-methylamphetamine, is a drug of the phenethylamine, amphetamine, and DOx families related to the psychedelic drug DOM.[1][3] It is the derivative of DOM in which the methoxy groups at the 2 and 5 positions have been replaced with ethoxy groups.[1] The properties and effects of DOM-2,5-DiEtO in humans do not appear to be known.[1][2] Similarly to DOM and DOET however, DOM-2,5-DiEtO has been reported to produce stimulant-like effects in rabbits.[3] The drug was patented by Alexander Shulgin as a potential "CNS stimulant" in 1970.[1][3] The chemical synthesis of DOM-2,5-DiEtO has been described.[1][3] Close analogues of DOM-2,5-DiEtO, besides DOM, include Florence (DOM-2-EtO) and Iris (DOM-5-EtO), as well as 2CD-2,5-DiEtO.[2][1]

See also

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References

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  1. 1 2 3 4 5 6 7 8 9 Shulgin A, Manning T, Daley PF (2011). The Shulgin Index, Volume One: Psychedelic Phenethylamines and Related Compounds. Vol. 1. Berkeley: Transform Press. ISBN 978-0-9630096-3-0.
  2. 1 2 3 4 5 Shulgin A, Shulgin A (September 1991). PiHKAL: A Chemical Love Story. Berkeley, California: Transform Press. ISBN 0-9630096-0-5. OCLC 25627628.
  3. 1 2 3 4 US 3547999A, Shulgin AT, "4-alkyl-dialkoxy-alpha-methyl-phenethylamines and their pharmacologically-acceptable salts", issued 15 December 1970, assigned to Dow Chemical Co.
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