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1.3- Diiodo-5,5-dimethylhydantoin

Dioxetanes. These unstable compounds have been isolated from the reactions of alkenes and singlet oxygen (5,487-488). Kopecky et al have reported a nonphotochemical route to 1,2-dioxetanes from (S-halo hydroperoxides, prepared by reaction in ether of an alkene, 98% HjOj, and 1,3-dibromo- or I, .l-diiodo-5,5-dimethylhydantoin (1, 208). Treatment of jS-halo hydroperoxides derived from trisubsLiluted olefins with sodium hydroxide in methanol at low lemperatures gives 1,2-dioxetanes, as formulated fortrimethyl-l,2-dioxetane (1) ... [Pg.531]

Di-n-iodo [2232-12-4]. 1,3-Diiodo-5,5-dime thy 1-2,4-imidazolidinedione. l,3-Diiodo-5,5-dimethylhydantoin C5HJ2N2O2 M 379.924... [Pg.419]

See other pages where 1.3- Diiodo-5,5-dimethylhydantoin is mentioned: [Pg.152]    [Pg.411]    [Pg.678]    [Pg.313]    [Pg.313]    [Pg.132]    [Pg.215]    [Pg.199]    [Pg.287]    [Pg.46]    [Pg.99]    [Pg.53]    [Pg.434]    [Pg.152]    [Pg.152]    [Pg.411]    [Pg.70]    [Pg.71]    [Pg.105]    [Pg.678]    [Pg.1008]   
See also in sourсe #XX -- [ Pg.199 ]

See also in sourсe #XX -- [ Pg.287 ]



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1.1- diiodo

5 : 5-Dimethylhydantoin

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