Talk:Trichloroisocyanuric acid

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Requested move

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)[reply]

SymcloseneTrichloroisocyanuric 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)[reply]

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The above discussion is preserved as an archive of the debate. Please do not modify it. Subsequent comments should be made in a new section on this talk page. No further edits should be made to this section.

From nitrile, needs verification

Nitriles can be obtained from primary amines via oxidation. Common methods include the use of Trichloroisocyanuric acid.[1]

References

  1. ^ 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?

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)[reply]