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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.
An ethoxy group (CH 3 CH 2 O−) is found in the organic compound ethyl phenyl ether (C 6 H 5 OCH 2 CH 3, also known as ethoxybenzene). Related to alkoxy groups are aryloxy groups , which have an aryl group singularly bonded to oxygen such as the phenoxy group ( C 6 H 5 O− ).
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).
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).
3-Methylhexane is a branched hydrocarbon with two enantiomers. [2] It is one of the isomers of heptane. The molecule is chiral, and is one of the two isomers of heptane to have this property, the other being its structural isomer 2,3-dimethylpentane. The enantiomers are (R)-3-methylhexane [3] and (S)-3-methylhexane. [4]
3-Methylhexane This page was last edited on 16 May 2022, at 14 ... Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; ...
Thioescaline (TE) is a pair of lesser-known psychedelic drugs with the chemical formula C 12 H 19 NO 2 S. They structural analogs of escaline in which an oxygen atom has been replaced with a sulfur atom.
C 3 H 4 O is a chemical formula that represents each of several actual and hypothetical compounds that differ in structure, but each consist of three atoms of carbon ...