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  2. 2,5-Dimethoxy-4-bromoamphetamine - Wikipedia

    en.wikipedia.org/wiki/2,5-Dimethoxy-4-bromo...

    The full name of the chemical is 2,5-dimethoxy-4-bromoamphetamine. DOB has a stereocenter and R -(−)-DOB is the eutomer . This is an important finding as it is suggestive that it is targeting different receptors relative to most other phenethylamines (e.g. MDMA ) where the R -isomer serves as the distomer .

  3. 6-MeO-DMT - Wikipedia

    en.wikipedia.org/wiki/6-MeO-DMT

    6-MeO-DMT, or 6-methoxy-N,N-dimethyltryptamine, also known as 6-OMe-DMT, is a serotonergic drug of the tryptamine family. [ 1 ] [ 2 ] It is the 6- methoxy derivative of the serotonergic psychedelic N , N -dimethyltryptamine (DMT) and is a positional isomer of the serotonergic psychedelic 5-MeO-DMT .

  4. 2C-B - Wikipedia

    en.wikipedia.org/wiki/2C-B

    2C-B (4-bromo-2,5-dimethoxyphenethylamine), also known as Nexus, is a synthetic psychedelic drug of the 2C family, mainly used as a recreational drug. [2] [1] [4] It was first synthesized by Alexander Shulgin in 1974 for use in psychotherapy.

  5. Bromomethane - Wikipedia

    en.wikipedia.org/wiki/Bromomethane

    Bromomethane, commonly known as methyl bromide, is an organobromine compound with formula C H 3 Br. This colorless, odorless, nonflammable gas is produced both industrially and biologically. It is a recognized ozone-depleting chemical. According to the IPCC Fifth Assessment Report, it has a global warming potential of 2. [5]

  6. Dimethylacetamide - Wikipedia

    en.wikipedia.org/wiki/Dimethylacetamide

    The chemical reactions of dimethylacetamide are typical of N,N-disubstituted amides. Hydrolysis of the acyl-N bond occurs in the presence of acids: CH 3 CON(CH 3) 2 + H 2 O + HCl → CH 3 COOH + (CH 3) 2 NH 2 + Cl −. However, it is resistant to bases. For this reason DMA is a useful solvent for reactions involving strong bases such as sodium ...

  7. Methedrone - Wikipedia

    en.wikipedia.org/wiki/Methedrone

    A reaction with methylamine in which the 2-bromo-1-(4-methoxyphenyl)propan-1-one becomes 1-(4-methoxyphenyl)-2-(methylamino)propan-1-ol. The final step is a reaction with potassium permanganate. The synthesis of mephedrone , a structurally similar compound with only one less ether group than methedrone, is well documented.

  8. Methoxyphenamine - Wikipedia

    en.wikipedia.org/wiki/Methoxyphenamine

    Methoxyphenamine (trade names ASMI, Euspirol, Orthoxine, Ortodrinex, Proasma), also known as 2-methoxy-N-methyl amphetamine (OMMA), is a β-adrenergic receptor agonist of the amphetamine class used as a bronchodilator. [1] It acts as an anti-inflammatory in rats. [2]

  9. 2-Bromo-4,5-methylenedioxyamphetamine - Wikipedia

    en.wikipedia.org/wiki/2-Bromo-4,5-methylenedioxy...

    2-Bromo-4,5-methylenedioxyamphetamine (6-Bromo-MDA) is a lesser-known psychedelic drug and a substituted amphetamine. It was first synthesized by Alexander Shulgin. In his book PiHKAL, the dose is listed as 350 mg and the duration unknown. [1] It produces stimulant effects but with no psychedelic or empathogenic action. [1]