Dianhydrohexitol dinitrates

Circular dichroism of the nitrato (ONO) chromophore of the mono- and di-nitric esters of l,4 3,6-dianhydrohexitols was found to consist of two dichroic bands, one weak and positive, at about 265 nm, and a stronger band at —228 nm, which was positive for the endo-(R)-nitrato chromophore and negative for the exo-(S)-nitrato group.68 However, for l,4 3,6-dianhydro-D-glucitol dinitrate, which has both an endo and an exo nitrato group, both bands were positive, but [ ]ma r (+ 7,260) for the band at 225 nm was about half of the algebraic sum of this band for the di-endo (+ 18,400) and di-exo (—4,460) compounds. 

Dinitrates of l,4 3,6-dianhydrohexitols have been prepared by Formann, Carr and Krantz [29] in an attempt to obtain vasodilatory substances. Jackson and Hayward [30] studied their chemical properties. 

Dulcitot hexanitiMe ( Nitrodulcitol ) D-Sorbitot bexanitrate Dinitrates of dianhydrohexitols Polyvinyl nitrate Literature... 

The double dehydration of sorbitol yields D-isosorbide (l,4 3,6-dianhydrohexitol), a white, biodegradable, nontoxic solid. It is used in medicine to treat glaucoma. Other medications are derived from isosorbide, including isosorbide dinitrate and isosorbide mononitrate used to treat angina pectoris. The high thermal stability makes isosorbide interesting as a monomeric building block for thermoplastic polymers such as polyester and polycarbonates. The electrophilic alkylation of isosorbide with dimethyl sulfate yields dimethyl isosorbide, a colorless liquid which is used as a plasticizer for vinyl polymers and as a solvent in pharmaceutical and cosmetic preparations. 

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