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3-Ethyl-2,4-dimethyloctane; 3-Ethyl-2,5-dimethyloctane; ... Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.
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).
This page was last edited on 18 November 2024, at 00:50 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.
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 .
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 ...
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Ethyl iodide (also iodoethane) is a colorless flammable chemical compound. It has the chemical formula C 2 H 5 I and is prepared by heating ethanol with iodine and phosphorus . [ 2 ] On contact with air, especially on the effect of light, it decomposes and turns yellow or reddish from dissolved iodine.