Chlorocyclopropane
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Chlorocyclopropane
Chlorocyclopropane is a organochlorine compound with the chemical formula . The compound is a member of haloalkane family. Synthesis The compound can be obtained by photoreaction of cyclopropane and chlorine gas; the reaction will generate polychlorinated compounds, which can be separated by physical means. Chemical properties The compound isomerizes on heating to 3-Chloropropene. Chlorocyclopropane reacts with lithium Lithium (from , , ) is a chemical element; it has chemical symbol, symbol Li and atomic number 3. It is a soft, silvery-white alkali metal. Under standard temperature and pressure, standard conditions, it is the least dense metal and the ... metal in ether to produce bicyclopropane. Also, it reacts with magnesium to obtain cyclopropylmagnesium chloride. See also * Chloroalkanes References {{Chlorine compounds Cyclopropyl compounds Organochlorides ...
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Fluorocyclopropane
Fluorocyclopropane is an organofluorine compound with the chemical formula . The compound is a member of haloalkane family. Synthesis The compound can be produced by reacting imidazolylidene cyclopropyl group with xenon difluoride. Also, a reaction of enantioselective cyclopropanation of fluoro-substituted allylic alcohols using zinc carbenoids. See also * Fluoroalkane Organofluorine chemistry describes the chemistry of organofluorine compounds, organic compounds that contain a carbon–fluorine bond. Organofluorine compounds find diverse applications ranging from oil and water repellents to pharmaceuticals, ...s * Fluorocyclohexane References Extra reading * * {{Fluorine compounds Cyclopropyl compounds Fluorine compounds Organofluorides ...
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Bromocyclopropane
Bromocyclopropane is a organobromine compound with the chemical formula . It is a member of haloalkane family. Synthesis The compound can be obtained by treating silver cyclopropanecarboxylate with bromine: : Chemical properties Reaction with magnesium, using diethyl ether as solvent, only gives about 25–30% of the cyclopropylmagnesium bromide Grignard reagent, with nearly as much cyclopropane formed by alternate reactions on the metal surface. The compound isomerizes on heating to produce 1-bromopropene and 3-bromopropene. Physical properties The compound is a flammable liquid that causes skin irritation and serious eye irritation. It is soluble in chloroform and methanol. Insoluble in water. See also * Bromoalkanes * Bromocyclohexane References

{{Bromine compounds Cyclopropyl compounds Organobromides ...
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