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Cyclohexanone 4- 0,1-dimethylethyl

Cyclohexanol, 4-ferr-butyl-, traits- [Cyclohexanol, 4-(l,l-dimethylethyl)-, traits-], 99 Cyclohexanone, 86... [Pg.139]

The formed hydroxyperoxide decomposes into free radicals much more rapidly than alkyl hydroperoxide [128]. So, the equilibrium addition of the hydroperoxide to the ketone changes the rate of formation of the radicals. This effect was first observed for cyclohexanone and 1,1-dimethylethyl hydroperoxide [128]. In this system, the rate of radical formation increases with an increase in the ketone concentration. The mechanism of radical formation is described by the following scheme ... [Pg.196]

Cyclohexanol. See Cyclohexanol Cyclohexanol acetate. See Cyclohexyl acetate Cyclohexanol, 4-t-butyl- Cyclohexanol, 4-(1,1-dimethylethyl)-. See 4-t-Butylcyclohexanol Cyclohexanol, 2-(1,1-dimethylethyl)-, acetate. See 2-t-Butylcyclohexyl acetate Cyclohexanol formate. See Cyclohexyl formate Cyclohexanol, 1 -((1-hydroperoxycyclohexyl) dioxy)-. See Cyclohexanone peroxide Cyclohexanol, 4,4 -isopropylidenedi-. See Bisphenol A, hydrogenated Cyclohexanol, 2-isopropyl-5-methyl-. See Menthol... [Pg.1120]

Peroxide, 1,1-dimethylethyl-1 -methyl-1 -phenylethyl. Seet-Butyl cumyl peroxide Peroxide, di-t-pentyl-. See Di-t-amyl peroxide Peroxide, 1-hydroperoxycyclohexyl 1-hydroxycyclohexyl-. See Cyclohexanone peroxide... [Pg.3266]

Synonyms 3-t-Butyl-5-chloro-6-methyl uracil 5-Chloro-3-t-butyl-6-methyluracil 5-Chloro-3-(1,1 -dimethylethyl)-6-methyl-2,4(1 H,3H)-pyrimidinedione 2,4 (1H,3H)-Pyrimidinedione, 5-chloro-3-(1,1-dimethylethyl)-6-methyl-Empirical C9H13CIN2O2 Properties Cryst. sol. in DMF, dimethyl acetamide, cyclohexanone mod. sol. in MIBK, butyl acetate, xylene sol. 710 ppm in water m.w. 216.69 m.p. 175 C... [Pg.4332]

Scheme 9.55. A representation of the reaction of 4-(l,l-dimethylethyl)cyclohexanone (4-f-butylcyclohexanone), with dimethylsulfonium methylide [(CH3)2S CH2 ]. Addition occurs primarily (ca. 80 20) from the axial direction and elimination of dimethyl sulfide [( 113)28] leads to the corresponding epoxide (oxirane). Scheme 9.55. A representation of the reaction of 4-(l,l-dimethylethyl)cyclohexanone (4-f-butylcyclohexanone), with dimethylsulfonium methylide [(CH3)2S CH2 ]. Addition occurs primarily (ca. 80 20) from the axial direction and elimination of dimethyl sulfide [( 113)28] leads to the corresponding epoxide (oxirane).

See other pages where Cyclohexanone 4- 0,1-dimethylethyl is mentioned: [Pg.99]    [Pg.267]    [Pg.62]    [Pg.102]    [Pg.601]    [Pg.130]    [Pg.4468]    [Pg.781]   
See also in sourсe #XX -- [ Pg.190 ]




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1.1- Dimethylethyl

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