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Cyclohexanes dihalo

It was characterized by chemical analysis, ozonolysis to form formaldehyde, hydrogenation, bromination and by its infrared and 1H-NMR spectra. The diene has also been prepared by pyrolysis of l,4-bis-(acetoxymethyl)cyclohexane (13,14), from cyclohexanedione by the Wittig reaction (11,15) or by reaction with diazomethane (16), and by the electrochemical or metal reduction of 1,4-dihalo-bicyclo-[2,2,2-]octanes (17,18) or of l,l,2,2-tetrakis-(bromo-methyl)-cyclobutane (19). It is very stable if stored in ammonia rinsed, dry flasks. [Pg.208]

Placido, J. Ortega, J. Excess enthalpies of 14 binary liquid mixtures of. alpha.,.omega.-dihalo(Cl, Br, I)alkanes (C2 - C6) + cyclohexane at 298.15 K. Experimental data and group contribution (DISQUAC) analysis of an extended database ELDATA Int. [Pg.657]


See other pages where Cyclohexanes dihalo is mentioned: [Pg.2382]    [Pg.2383]    [Pg.2424]    [Pg.1213]   
See also in sourсe #XX -- [ Pg.2 , Pg.143 ]




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