Talk:Trichloroisocyanuric acid
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Requested move
[edit]- The following discussion is an archived debate of the proposal. Please do not modify it. Subsequent comments should be made in a new section on the talk page. No further edits should be made to this section.
The result of the debate was uncontroversial, thus moved Patstuarttalk|edits 19:08, 3 January 2007 (UTC)
Symclosene → Trichloroisocyanuric acid — Google search gives 551 hits for symclosene and +69,000 for trichloroisocyanuric acid. Also consistent with current naming of cyanuric acid, a "parent" chemical compound. Previously discussed at User talk:Smokefoot#Symclosene and dichlor and User talk:Fvasconcellos#Symclosene and dichlor. Fvasconcellos 17:20, 27 December 2006 (UTC) Fvasconcellos 17:20, 27 December 2006 (UTC)
Survey
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[edit]Discussion
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Nitriles can be obtained from primary amines via oxidation. Common methods include the use of Trichloroisocyanuric acid.[1]
References
- ^ Chen, Fen-Er; Kuang, Yun-Yan; Hui-Fang, Dai; Lu, Liang (2003). "A Selective and Mild Oxidation of Primary Amines to Nitriles with Trichloroisocyanuric Acid". Synthesis. 17 (17): 2629–2631. doi:10.1055/s-2003-42431..
Trichloride explosive?
[edit]Can this common chemical react with ammonia to create nitrogen trichloride, an unstable explosive when in concentrated form? The article does not mention this. David Spector (talk) 12:15, 25 December 2021 (UTC)