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3-Ethyl-5,5-dimethyloctane; 4-Ethyl-2,2-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 .
1.624 g/mL Boiling point: 180 °C (356 °F; 453 K) Solubility in water. Insoluble Hazards ... Text is available under the Creative Commons Attribution-ShareAlike 4.0 ...
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4-Iodophenol (p-iodophenol) is an aromatic organic compound. A colorless solid, it is one of three monoiodophenols. 4-Iodophenol undergoes a variety of coupling reactions in which the iodine substituent is replaced by a new carbon group para to the hydroxy group of the phenol . [ 3 ]