MDOH
Chemistry
- Formula
- C10H13NO3
- Molar mass
- 195.21 g/mol
- IUPAC name
- N-[1-(1,3-benzodioxol-5-yl)propan-2-yl]hydroxylamine
- InChIKey
- FNDCTJYFKOQGTL-UHFFFAOYSA-N
Chemistry from PubChem CID 98528.
Also known as
- N-Hydroxy mda
- N-Hydroxy-3,4-methylenedioxyamphetamine
- 74698-47-8
- N-OH-Mda
- N-Hydroxy methylenedioxyamphetamine
- SJE1T2B1A7
- N-Hydroxy-1-(3,4-methylenedioxyphenyl)-2-aminopropane
- 1,3-Benzodioxole-5-ethanamine, N-hydroxy-alpha-methyl-
Stereoisomers
2 distinct stereoisomers are registered for this structure. This area's record is the racemate — the mixture, which is normally the form encountered.
- N-hydroxy-3,4-methylenedioxyamphetamine this area mixture CID 98528
- N-Hydroxy-3,4-methylenedioxyamphetamine, (R)- CID 57504054
- N-Hydroxy-3,4-methylenedioxyamphetamine, (S)- CID 92178775
Attribution
Alexander "Sasha" Shulgin — discovered its activity, 1991
Human activity is documented by Shulgin in PiHKAL (#114), but the original synthesizer is not clearly documented and the first-human-report claim could not be confirmed from fetched sources; it may trace to Braun, Shulgin and Braun's 1980 study of N-substituted MDA analogs.
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