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・ 1,2,3-Triazole
・ 1,2,3-Tribromopropane
・ 1,2,3-Trichloropropane
・ 1,2,3-Trimethylbenzene
・ 1,2,3-Trinitrobenzene
・ 1,2,4-Butanetriol
・ 1,2,4-Butanetriol trinitrate
・ 1,2,4-Triazole
・ 1,2,4-Trichlorobenzene
・ 1,2,4-Trihydroxyanthraquinone
・ 1,2,4-Trimethylbenzene
・ 1,2,4-Trioxane
・ 1,2,6-Trigalloyl glucose
・ 1,2-alpha-L-fucosidase
・ 1,2-alpha-mannosidase
1,2-Benzenedithiol
・ 1,2-Benzoquinone
・ 1,2-Bis(dicyanomethylene)squarate
・ 1,2-Bis(diisopropylphosphino)ethane
・ 1,2-Bis(dimethylarsino)benzene
・ 1,2-Bis(dimethylphosphino)ethane
・ 1,2-Bis(diphenylphosphino)ethane
・ 1,2-Butanediol
・ 1,2-Butylene carbonate
・ 1,2-Cyclohexane dicarboxylic acid diisononyl ester
・ 1,2-dehydroreticulinium reductase (NADPH)
・ 1,2-diacylglycerol 3-glucosyltransferase
・ 1,2-Diaminopropane
・ 1,2-Diazepine
・ 1,2-Dibromo-3-chloropropane


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1,2-Benzenedithiol : ウィキペディア英語版
1,2-Benzenedithiol

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1,2-Benzenedithiol is the organosulfur compound with the formula C6H4(SH)2. This colourless viscous liquid consists of a benzene ring with a pair of adjacent thiol groups. The conjugate base of this diprotic compound serves as chelating agent in coordination chemistry and a building block for the synthesis of other organosulfur compounds.〔Karlin, K. D.; Stiefel, E. I., Eds. “Progress in Inorganic Chemistry, Dithiolene Chemistry: Synthesis, Properties, and Applications” Wiley-Interscience: New York, 2003. ISBN 0-471-37829-1〕
==Synthesis==
The compound is prepared by ortho-lithiation of benzenethiol using butyl lithium (BuLi) followed by sulfidation:
:C6H5SH + 2 BuLi → C6H4SLi-2-Li + 2 BuH
:C6H4SLi-2-Li + S → C6H4(SLi)2
:C6H4(SLi)2 + 2 HCl → C6H4(SH)2 + 2 LiCl
The compound was first prepared from 2-aminobenzenethiol via diazotization. Alternatively, it forms from 1,2-dibromobenzene.

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