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Ethyl phosphorodichloridate

Detailed interpretations of the n.m.r. spectra of vinylphosphonic acid," phosphoenolpyruvate, and some TV -phosphorylaziridines have been carried out. The vibrational spectra of ethyl phosphorodichloridate and its 1,1-dideuterio- and 2,2,2-trideuterio-derivatives have been examined. [Pg.120]

The disadvantage of this method, especially for large-scale work, lies in the utilization of large quantities of pyridine. Furthermore, with ethyl alcohol some ethyl phosphorodichloridate (II) is usually produced even under conditions favourable to the production of diethyl phosphorochloridate. [Pg.57]

Compound Name Ethylhexaldehyde N-Propyl Alcohol Diethyl Carbonate Ethyl Chloracetate Ethyl Chloride Ethyl Chloroacetate Ethyl Chloroformate Ethyl Chloroacetate Ethyl Chloroacetate Ethyl Phosphorodichloridate Ethyldichlorosilane Ethylene... [Pg.50]

Ethyl Phosphorodichloridate Diethyl Phthalate Methylethylpyridine Ethyl Acrylate 2-Ethyl-3-Propylacrolein 2-Ethyl-3-Propylacrolein Tetraethyl Pyrophosphate Ethyl Silicate Ethyl Silicate Ethyl Silicate Ethyltrichlorosilane Ethyltrichlorosilane Ethyl Mercaptan... [Pg.52]

Prophos is prepared by the reaction of ethyl phosphorodichloridate with /i-propylmercaptan in aqueous sodium hydroxide. [Pg.258]

ETHYL PHOSPHORODICHLORIDATE (1498-51-7) May be combustible. Reacts with moisture in air, forming hydrogen chloride. Reacts with water, steam, forming hydrochloric acid. Incompatible with strong acids, strong oxidizers, nitrates. Aqueous solution incompatible with sulfuric acid, alkalis, ammonia, aliphatic amines, alkanolamines, alkylene oxides, amides, epiehlorohydrin, organic anhydrides, isocyanates, vinyl acetate. Attacks some plastics, rubber, and coatings. Attacks metals in the presence of moisture. [Pg.545]

Dichloroethoxyphosphine oxide Dichlorophosphoric acid, ethyl ester EINECS 216-099-0 Ethyl dichlorophosphate Ethyl phosphorodichloridate HSDB 417 NA2927 NSC 87631 Phosphorodichloridic acid, ethyl ester. Liquid bpio = 60-65". [Pg.278]

Ethyl phosphorodichloridate added with cooling at room temp, to an emulsion of 1,3-propanediol in a soln. of 2 moles of triethylamine in benzene, and the reaction allowed to proceed overnight at room temp. ethyl propylene phosphate. Y 80%. F. e. s. M.-T. Boisdon, A. Munoz, and J.-P. Vives, G. r. 253, 1570 (1961). [Pg.339]

Phosphorus Pentasulfide Ethyl Phosphorodichloridate Plumbous Fluoride Lead Fluoride... [Pg.159]

CALCIUM HYPOCHLORITE, dry, includii mixtures with more than 39% 1760 60 ETHYL PHOSPHORODICHLORIDATE... [Pg.758]

Ethyl phosphorodichloridate Ethylphosphoric acid dichloride CgHgCIgOgP 1498-51-7 162.940 62 " 1.4338 " ... [Pg.409]

Ethylphosphonic acid Ethyl phosphorodichloridate 5-EViyl-2-piccline... [Pg.410]

See other pages where Ethyl phosphorodichloridate is mentioned: [Pg.657]    [Pg.57]    [Pg.52]    [Pg.76]    [Pg.368]    [Pg.175]    [Pg.644]    [Pg.66]    [Pg.487]    [Pg.487]    [Pg.278]    [Pg.702]    [Pg.736]    [Pg.367]    [Pg.44]    [Pg.65]    [Pg.146]    [Pg.312]    [Pg.538]    [Pg.720]    [Pg.780]    [Pg.839]    [Pg.354]    [Pg.401]    [Pg.367]   
See also in sourсe #XX -- [ Pg.44 , Pg.84 ]

See also in sourсe #XX -- [ Pg.368 ]

See also in sourсe #XX -- [ Pg.384 ]

See also in sourсe #XX -- [ Pg.44 , Pg.84 ]

See also in sourсe #XX -- [ Pg.44 , Pg.84 ]



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Phosphorodichloridates

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