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Trichloroisocyanuric add

Trichloroisocyanuric add, CjCljNjOs (mp 249-251 °C), converts ethers into esters [722], and sodium iV-chloro-/>-tolnenesulfonamide (Chlo-ramine-T),/>-CH3C4H4S02NCINa 3H20 (mp 167-170 °C), in the presence of osmium tetroxide, transforms alkenes into vicinal hydroxy sulfonamido compounds [723]. [Pg.28]

Chlorotrimethylsilane can be added to alkenes to give alkyl chlorides. 1-Hexene reacts with MesSiCl in water to give 2-chlorohexane. Treatment of an alkene with KHF2 and SLF4 leads to the alkyl fluoride, and bromotrimethylsilane adds to alkynes to give the vinyl bromide. Trichloroisocyanuric acid reacts with terminal alkenes in water to give the 1-chloro alkane. ... [Pg.1031]

See other pages where Trichloroisocyanuric add is mentioned: [Pg.365]    [Pg.150]    [Pg.54]    [Pg.587]    [Pg.365]    [Pg.150]    [Pg.54]    [Pg.587]    [Pg.385]   
See also in sourсe #XX -- [ Pg.110 ]



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