Boron oxide phosgene

Phenylhydrazine Phosgene Phosphine Lead dioxide, oxidizers Aluminum, alkali metals, 2-propanol Air, boron trichloride, bromine, chlorine, nitric acid, nitrogen oxides, nitrous acid, oxygen, silver nitrate... 

Liquid perchloryl fluoride is a typical nonpolar solvent. Most inorganic and organic salts are insoluble in it. Conversely, most covalent, essentially nonpolar substances, boiling within about 50°G of perchloryl fluoride, are completely miscible, e.g., chlorine, boron trifluoride, sulfur hexafluoride, silicon tetrafluoride, phosgene, nitrous oxide, chlorine trifluoride, chlorofluorocarbons, silicon tetrachloride, sulfuryl chloride, dinitrogen tetroxide, and thionyl chloride 106). 

The addition of a gas to a reaction mixture (commonly the hydrogen halides, fluorine, chlorine, phosgene, boron trifluoride, carbon dioxide, ammonia, gaseous unsaturated hydrocarbons, ethylene oxide) requires the provision of safety precautions which may not be immediately apparent. Some of these gases may be generated in situ (e.g. diborane in hydroboration reactions), some may be commercially available in cylinders, and some may be generated by chemical or other means (e.g. carbon dioxide, ozone). An individual description of the convenient sources of these gases will be found under Section 4.2. 

Carbonyl bromide, or bromophosgene, was prepared for the first time by Emmerling by the oxidation of bromoform with potassium dichromate and sulphuric acid. Later it was also obtained by heating boron bromide to 150° C. with phosgene, but by this method a mixture with other compounds is obtained ... 

The reaction between boron(III) oxide (or boric acid, borax, kernite or colemanite) and phosgene in a molten salt (AlClj/NaCI) has been patented as a commercial route to boron(III) chloride [148] ... 

One of the serious drawbacks of the Wittig reaction is the unavoidable production of triphenylphosphane oxide in stoichiometric quantities. Whilst its direct reduction with boron, aluminium or silicon hydrides would be possible, these reagents are too expensive for a viable process. In fact, distilled triphenylphosphane oxide is reacted with phosgene, generated in situ, to give the corresponding dichloride, which is then reduced with metals, like aluminium. [55]... 

Carbonothioic acid, 0-(6-chloro-3-phenyl-4-pyridazinyl) S-octyl ester. See Pyridate, Carbonothioic dichloride. See Thiophosgene Carbon oxide. See Carbon monoxide Carbon oxide sulfide. See Carbonyl sulfide Carbon oxychloride. See Phosgene Carbon oxysulfide. See Carbonyl sulfide Carbon silicide. See Silicon carbide Carbon sulfide. See Carbon disulfide Carbon tet. See Carbon tetrachloride Carbon tetraboride. See Boron carbide Carbon tetrabromide CAS 558-13-4 EINECS/ELINCS 209-189-6 UN 2516... 

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