Search results
Results from the WOW.Com Content Network
Tetraethoxymethane can be used as a solvent and for the alkylation of CH-acidic compounds (e.g. phenols and carboxylic acids).In addition, it reacts with amines, enol ethers and sulfonamides, [12] whereby spiro compounds can also be obtained.
The longest possible main alkane chain is used; therefore 3-ethyl-4-methylhexane instead of 2,3-diethylpentane, even though these describe equivalent structures. The di-, tri- etc. prefixes are ignored for the purpose of alphabetical ordering of side chains (e.g. 3-ethyl-2,4-dimethylpentane, not 2,4-dimethyl-3-ethylpentane).
Ethylvanillin can be methylate to 4-ethoxy-3-methoxybenzladehyde. The 4-ethoxy-3-methoxybenzaldehyde is then subjected to a Bayer-Villiger oxidation with peracetic acid and acetic acid to yield 4-ethoxy-3-methoxyphenol. The 4-ethoxy-3-methoxyphenol is methylated to yield 2,4-dimethoxy-1-ethoxybenzene. The 2,4-dimethoxy-1-ethoxybenzene is ...
3-Methylhexane This page was last edited on 16 May 2022, at 14:52 (UTC). Text is available under the Creative Commons Attribution-ShareAlike 4.0 ...
The structure of a typical methoxy group. In organic chemistry, a methoxy group is the functional group consisting of a methyl group bound to oxygen.This alkoxy group has the formula R−O−CH 3.
TME, or thio metaescaline, is a series of lesser-known psychedelic drugs similar in structure to mescaline.Their structures are based on that of metaescaline.They were first synthesized by Alexander Shulgin and recorded in his book PiHKAL (Phenethylamines i Have Known And Loved).
It consists of a methylene bridge (−CH 2 − unit) bonded to a hydroxyl group (−OH). This makes the hydroxymethyl group an alcohol . It has the identical chemical formula with the methoxy group ( −O−CH 3 ) that differs only in the attachment site and orientation to the rest of the molecule.
Main page; Contents; Current events; Random article; About Wikipedia; Contact us; Help; Learn to edit; Community portal; Recent changes; Upload file