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lic 6 h 4 ch 2 n(ch 3) 2 + e + → 2-ec 6 h 4 ch 2 n(ch 3) 2 Via these reactions, many derivatives are known with the formula 2-X-C 6 H 4 CH 2 N(CH 3 ) 2 (E = SR, PR 2 , etc.). The amine is basic and undergoes quaternization with alkyl halides (e.g. hexyl bromide ) to give quaternary ammonium salts: [ 4 ]
para-Chloromethamphetamine (also known as 4-chloromethamphetamine and 4-CMA) is a stimulant that is the N-methyl derivative and prodrug of the neurotoxic drug para-chloroamphetamine (4-CA). [ 1 ] [ 2 ] It has been found to decrease serotonin in rats.
The secondary functional groups are: a hydroxy- at carbon 5, a chloro- at carbon 11, a methoxy- at carbon 15, and a bromo- at carbon 18. Grouped with the side chains, this gives 18-bromo-12-butyl-11-chloro-4,8-diethyl-5-hydroxy-15-methoxy. There are two double bonds: one between carbons 6 and 7, and one between carbons 13 and 14.
4-Chloromethcathinone (also known as 4-CMC and clephedrone) is a stimulant drug of the cathinone class that has been sold online as a designer drug. [ 1 ] [ 2 ] 4-CMC produces similar effects to mephedrone , and has been sold as an alternative in countries where mephedrone was scheduled.
In organic chemistry, xylene or xylol (from Greek ξύλον (xylon) 'wood'; [1] [2] IUPAC name: dimethylbenzene) are any of three organic compounds with the formula (CH 3) 2 C 6 H 4. They are derived from the substitution of two hydrogen atoms with methyl groups in a benzene ring; which hydrogens are substituted determines which of three ...
DMTMM (4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methyl-morpholinium chloride) is an organic triazine derivative commonly used for activation of carboxylic acids, particularly for amide synthesis. Amide coupling is one of the most common reactions in organic chemistry and DMTMM is one reagent used for that reaction.
4'-Chlorodeschloroalprazolam is a triazolobenzodiazepine derivative which has been sold as a designer drug, presumably with sedative effects, first identified in Australia and the US in 2021, [1] [2] and subsequently in Ireland.
The 5-chloro-2,1,3-benzothiadiazol-4-amine intermediate was a known compound, produced in three steps from 4-chlorophenylenediamine as shown. [18] Treatment with two equivalents of thionyl chloride in pyridine formed the heterocycle , which was nitrated with sodium nitrate in sulfuric acid and reduced using iron and acetic acid.