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The page provides a comprehensive list of isomers of dodecane, including their chemical structures and properties.
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 .
IDNNA (2,5-dimethoxy-4-iodo-N,N-dimethylamphetamine) is a lesser-known psychedelic drug and a substituted amphetamine. It is also the N,N-dimethyl analog of DOI. IDNNA was first synthesized by Alexander Shulgin. In his book PiHKAL, the minimum dosage is listed as 2.6 mg, and the duration unknown. [1] IDNNA produces few to no effects.
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).
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The company's 3.2% dividend yield and 5.97% five-year dividend growth rate provide a compelling mix of current income and future growth potential, even with its elevated 93.2% payout ratio.
Monoiodotoluene isomers [1] [2] [3] Common name Structure Systematic name: 1-iodo-2-methylbenzene 1-iodo-3-methylbenzene 1-iodo-4-methylbenzene Other names 2-iodotoluene 3-iodotoluene 4-iodotoluene Molecular formula: C 7 H 7 I (C 6 H 4 ICH 3) Molar mass: 218.03 g/mol Appearance Clear dark brown liquid white to yellow solid