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2,5-Dimethoxy-4-iodoamphetamine (DOI) is a psychedelic drug and a substituted amphetamine. Unlike many other substituted amphetamines, however, it is not primarily a stimulant . [ 3 ] DOI has a stereocenter and R -(−)-DOI is the more active stereoisomer .
3-Ethyl-2,2-dimethyloctane; 3-Ethyl-2,3-dimethyloctane; 3-Ethyl-2,4-dimethyloctane; 3-Ethyl-2,5-dimethyloctane; 3-Ethyl-2,6-dimethyloctane; 3-Ethyl-2,7-dimethyloctane
3-Ethyl-2-methylundecane; 3-Ethyl-3-methylundecane; 3-Ethyl-4-methylundecane; 3-Ethyl-5-methylundecane; 3-Ethyl-6-methylundecane; 3-Ethyl-7-methylundecane
The parent isoindole was prepared by flash vacuum pyrolysis of an N-substituted isoindoline. [5] N-Substituted isoindoles, which are easier to handle, can be prepared by dehydration of isoindoline-N-oxides. They also arise by myriad other methods, e.g., starting from xylylene dibromide (C 6 H 4 (CH 2 Br) 2).
3-Methoxymethcathinone (3-MeOMC), also known as meta-methoxymethcathinone (m-MeOMC), is a designer drug of the substituted cathinone family described as a stimulant. [ 3 ] [ 2 ] [ 1 ] Similarly to other cathinones, it acts as a monoamine releasing agent , including of serotonin , dopamine , and norepinephrine .
Daughter Admits She Used to Throw Plates Away Rather Than Clean Them Up — See How Her Parents Reacted
2,5-Dimethoxy-4-ethylamphetamine (DOET, DOE, Hecate) is a psychedelic drug of the phenethylamine and amphetamine chemical classes. It was first synthesized by Alexander Shulgin , and was described in his book PiHKAL ( Phenethylamines i Have Known And Loved ).