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Acetosyringone or 1-(4-Hydroxy-3,5-dimethoxyphenyl)-ethanone or 4′-Hydroxy-3′,5′-dimethoxyacetophenone Formula: C10H12O4 CAS#:2478-38-8 MW: 196.2
3,4-Di methoxy phenethylamine (DMPEA) is a chemical compound of the phenethylamine class. It is an analogue of the major human neurotransmitter dopamine where the 3- and 4-position hydroxy groups have been replaced with methoxy groups. It is also closely related to mescaline which is 3,4,5-trimethoxyphenethylamine.
Acetophenone is formed as a byproduct of the cumene process, the industrial route for the synthesis of phenol and acetone.In the Hock rearrangement of isopropylbenzene hydroperoxide, migration of a methyl group rather than the phenyl group gives acetophenone and methanol as a result of an alternate rearrangement of the intermediate:
It has binding affinity towards 5-HT2C and 5-HT2A receptors in rats. [3] It features competitive antagonist activity at 5-HT serotonin receptor in Sprague-Dawley rat stomachs. [ 3 ] It exhibits binding affinity against rat 5-hydroxytryptamine 2C receptors using [3H] mesulergine as a radioligand.
C 16 H 16 O 3: Molar mass: 256.301 g·mol −1 Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], ...
3,4-Dihydroxyphenylacetic acid (DOPAC) is a metabolite of the neurotransmitter dopamine. Dopamine can be metabolized into one of three substances. One such substance is DOPAC. Another is 3-methoxytyramine (3-MT). Both of these substances are degraded to form homovanillic acid (HVA).
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2,5-Dimethoxyamphetamine is listed as a Scheduled I controlled substance at the federal level in the United States and is therefore illegal to buy, possess, and sell. [ 4 ] 2,4-dimethoxyamphetamine, 2,6-dimethoxyamphetamine, 3,4-dimethoxyamphetamine, and 3,5-dimethoxyamphetamine are each position isomers of 2,5-dimethoxyamphetamine, they are ...