翻訳と辞書 ・ 1,2-Dihydro-1,2-azaborine ・ 1,2-dihydrovomilenine reductase ・ 1,2-dihydroxy-6-methylcyclohexa-3,5-dienecarboxylate dehydrogenase ・ 1,2-dihydroxynaphthalene dioxygenase ・ 1,2-Diiodoethane ・ 1,2-Dimethoxybenzene ・ 1,2-Dimethylcyclopropane ・ 1,2-Dimethylhydrazine ・ 1,2-dioleoyl-sn-glycerophosphoethanolamine ・ 1,2-Dioxane ・ 1,2-Dioxetane ・ 1,2-Dioxetanedione ・ 1,2-Dioxin ・ 1,2-Dithietane ・ 1,2-Dithiole ・ 1,2-Ethanedithiol ・ 1,2-Naphthoquinone ・ 1,2-Propanedithiol ・ 1,2-rearrangement ・ 1,2-Wittig rearrangement ・ 1,227 QI Facts to Blow Your Socks Off ・ 1,3,2,4-Dithiadiphosphetane 2,4-disulfides ・ 1,3,3,3-Tetrafluoropropene ・ 1,3,5-Triazido-2,4,6-trinitrobenzene ・ 1,3,5-Triazine ・ 1,3,5-Trichlorobenzene ・ 1,3,5-Trinitrobenzene ・ 1,3,5-Trioxane ・ 1,3,5-Trioxanetrione ・ 1,3,5-Trithiane
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1,2-Ethanedithiol : ウィキペディア英語版 | 1,2-Ethanedithiol
|Section2= |Section3= |Section7= |Section8= }} 1,2-Ethanedithiol is a colorless liquid with the formula C2H4(SH)2. It has a very characteristic odor which is compared by many people to rotten cabbage. It is a common building block in organic synthesis and an excellent ligand for metal ions. ==Preparation== 1,2-Ethanedithiol is prepared commercially by the reaction of 1,2-dichloroethane with aqueous sodium bisulfide. In the laboratory, it can also be prepared by the action of 1,2-dibromoethane on thiourea followed by hydrolysis.
抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)』 ■ウィキペディアで「1,2-Ethanedithiol」の詳細全文を読む
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