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3-Methoxy-4-methylamphetamine (MMA) is an entactogen and psychedelic drug of the phenethylamine and amphetamine classes. [ 1 ] [ 2 ] It was first synthesized in 1970 [ 1 ] and was encountered as a street drug in Italy in the same decade. [ 3 ]
3-Methoxy-4-ethoxyphenethylamine (MEPEA) is a lesser-known psychedelic drug. It was first synthesized by Alexander Shulgin. In his book PiHKAL (Phenethylamines i Have Known And Loved), the minimum dosage is listed as 300 mg, and the duration unknown. [1] MEPEA is said to produce a light lifting feeling and a +1 on the Shulgin Rating Scale. Very ...
The longest possible main alkane chain is used; therefore 3-ethyl-4-methylhexane instead of 2,3-diethylpentane, even though these describe equivalent structures. The di-, tri- etc. prefixes are ignored for the purpose of alphabetical ordering of side chains (e.g. 3-ethyl-2,4-dimethylpentane, not 2,4-dimethyl-3-ethylpentane).
Ethylvanillin can be methylate to 4-ethoxy-3-methoxybenzladehyde. The 4-ethoxy-3-methoxybenzaldehyde is then subjected to a Bayer-Villiger oxidation with peracetic acid and acetic acid to yield 4-ethoxy-3-methoxyphenol. The 4-ethoxy-3-methoxyphenol is methylated to yield 2,4-dimethoxy-1-ethoxybenzene. The 2,4-dimethoxy-1-ethoxybenzene is ...
TME, or thio metaescaline, is a series of lesser-known psychedelic drugs similar in structure to mescaline.Their structures are based on that of metaescaline.They were first synthesized by Alexander Shulgin and recorded in his book PiHKAL (Phenethylamines i Have Known And Loved).
3-Methylhexane This page was last edited on 16 May 2022, at 14:52 (UTC). Text is available under the Creative Commons Attribution-ShareAlike 4.0 ...
7,8-didehydro-4,5-α-epoxy- 3-ethoxy-17-methylmorphinan-6-α-ol. CAS Number: ... 100.000.883: Chemical and physical data; Formula: C 19 H 23 N O 3: Molar mass: 313. ...
The structure of a typical methoxy group. In organic chemistry, a methoxy group is the functional group consisting of a methyl group bound to oxygen.This alkoxy group has the formula R−O−CH 3.