Search results
Results from the WOW.Com Content Network
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.
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.
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).
Main page; Contents; Current events; Random article; About Wikipedia; Contact us; Help; Learn to edit; Community portal; Recent changes; Upload file
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 ...
Get AOL Mail for FREE! Manage your email like never before with travel, photo & document views. Personalize your inbox with themes & tabs. You've Got Mail!
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 ...