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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 page provides a comprehensive list of isomers of dodecane, including their chemical structures and properties.
Diiodomethane is a reagent for installing the CH 2 group. In the Simmons–Smith reaction, it is a source of methylene. [4] In fact the Simmons–Smith reaction does not produce free carbene but proceeds via Zn-CH 2 I intermediates. Diiodomethane is also a source of the equivalent of CH 2+ 2. The synthesis of Fe 2 (CH 2)(CO) 8 illustrates this ...
Tetraiodoethylene (TIE), or diiodoform, is the periodinated analogue of ethylene with the chemical formula C 2 I 4. It is a decomposition product of carbon tetraiodide and diiodoacetylene . [ 5 ] It is an odourless yellow crystalline solid that is soluble in benzene and chloroform , and insoluble in water. [ 2 ]
Substituted phenethylamines (or simply phenethylamines) are a chemical class of organic compounds that are based upon the phenethylamine structure; [note 1] the class is composed of all the derivative compounds of phenethylamine which can be formed by replacing, or substituting, one or more hydrogen atoms in the phenethylamine core structure with substituents.
Idoxuridine is available as either a 0.5% ophthalmic ointment or as a 0.1% ophthalmic solution. [3] The dosage of the ointment is every 4 hours during day and once before bedtime. [ 3 ] The dosage of the solution is 1 drop in the conjunctival sac hourly during the day and every 2 hours during the night until definitive improvement, then 1 drop ...