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3,5-diphenyl- -chloride

Diphenyl- -chlorid-chlorsulfonylimid E2, 290 Diphenyl- -chlorid-( 1-cyan-l-methyl-cthylimid)... [Pg.1022]

Diphenyl- -chlorid-dichloracetylimid E2, 29 I Diphenyl- -chlorid-(diphenvlphosphinyljmid) E2, 289... [Pg.1022]

Diphenyl- -chlorid-(4-nitro-benzoylimid) E2, 289 Diphenyl- -chlorid-phenylimid XU/1, 291 E2, 96, 288, 297... [Pg.1022]

Diphenyl- -chlorid-phenylsulfonylimid E2, 290 Diphenyl- -chlorid-tosylimid E2, 289 Diphenyl- -chlorid-trichloracetylimid E2, 290 Diphenyl- -(1-cyan-ethylester) E2, 211 Diphenyl- -cyclohexylester E2, 219 Diphenyl- -cyanureid XII/1, 263 Diphenyl- -dichloracetylamid E2, 240 Diphenyl- -(1,2-dicthoxycarbonyl-hvdrazid) E2, 239 Diphenyl- -diethylamid E2, 230, 233 Diphenvl- -(1,2-dimethoxycarbonyl-hydrazid) E2, 239 ... [Pg.1022]

Ammoninm Chlormethylen-diphenyl- (chlorid) E5, 39/42 (OHC —NAr2 -f Cl-COCO-Cl)... [Pg.1113]

Indium triciilor-ide. Indium diphenyl chloride. Goddard and Goddard, uupub iished. [Pg.76]

Thallic chloride. Ether or benzene solution. Thallium diphenyl chloride, phenyimercurio chloride. Goddard, Tram. Clicm. Bor. 1922, 121, 40,... [Pg.76]

The type R BX is represented by boron diphenyl chloride and bromide, both being prepared by the use of mercury diphenyl. The chloride is a liquid, B.pt. 270" to 271" C., and the bromide a solid, M.pt, 24" to 25 C. Treatment with sodium hydroxide yields the type R2B.OII. [Pg.220]

The metal indium has so far only yielded one derivative, indium diphenyl chloride. This was isolated by the interaction of mercury diphenyl and metallic indium in boiling xylene. It is an insoluble compound, not melting at 350 C. When metallic indium and mercury diphenyl are heated at 270 C. in a nitrogen atmosphere under reduced... [Pg.220]

Diphenyl boric acid, Ph B.OH. —When boron diphenyl chloride or bromide is treated mth sodium hydroxide, and the clear solution... [Pg.228]

Indium diphenyl chloride.—Indium trichloride Irom 1-lC grams of metallic indium, and 10-77 grams of mercury diphenyl (3 mols.) are boiled with 50 c.c, of xylene for thirty-seven hours. After filtering, the residue mostly melts at 245" to 250 " C., but a portion does not melt at 295° C. The mass is extracted in a Soxhiet apparatus with dr benzene to remove any mercury compounds, and the residue in the thimble (0 647gram) is organic and found to be indium diphenyl chloride. It is a crystalline, cream-coloured powder, insoluble in the usual organic solvents, and does not melt at 350° C. [Pg.235]

Tin diphenyl aminochloride, Sn(C6H5)aNH2Cl, is formed as a by-product in the preparation of tin triphenyl chloride from tin diphenyl chloride by the action of ammonia. When treated with water it is decomposed into tin diphenyl hydroxychloride and ammonia. [Pg.325]

The body shows decomposition if heated above 270° C. and burns in air with a reddish flame and the separation of lead oxide. It is moderately soluble in chloroform, benzene, or carbon bisulphide when hot, and difficultly soluble in alcohol, ether, ligroin, or acetic acid. If heated in a sealed tube with hydrochloric acid decomposition occurs, lead tetrachloride and benzene being produced. By the action of halogens or concentrated nitric acid two phenyl groups are split off, and a lead diphenyl dihalide or dinitrate formed. A similar action takes place with iodic acid, formic, acetic, trichloracetic, propionic, valeric, and p-nitrobenzoic acids. With metallic chlorides the following derivatives are formed arsenic trichloride — lead diphenyl dichloride and diphenyl arsenious chloride antimony trichloride — lead diphenyl dichloride and diphenylstibine chloride antimony penta-chloride — lead diphenyl dichloride and diphenylstibine trichloride bismuth tribromide —> lead diphenyl dichloride and diphenylchloro-bismuthine thallie chloride —> lead diphenyl dichloride and thallium diphenyl chloride tellurium tetrachloride —> lead diphenyl dichloride and tellurium diphenyl dichloride. [Pg.340]

Lead triethyl chloride, thallous chloride, methyl chloride Lead diethyl dichloride, thallous chloride, ethyl chloride. Thallium diphenyl chloride, mercuric chloride. Benzylmercm-io oldoride, thallous chloride. [Pg.360]

Thallium diphenyl chloride, tin triphenyl chloride, tin diphenyl hydroxychloride, hydrochloric acid. [Pg.360]

Thallium diphenyl chloride, lead diphenyl dichloritle. Lead di-m xylyl dichloride, thallous chloride. [Pg.360]

Thallium diphenyl chloride, lead diethyl dichloridt . Thallium di-a-naphthyl chloride, load diphenyl dichloride. [Pg.360]

Thallium diphenyl chloride, diphenyichlorobismutliiiu. Thallium di-p-tolyl chloride, dLp-tolylchlorobismuthine thallium di-a-naphthyl chloride, di-a-naphthylchioro-bismuthine. [Pg.360]

CH2CH2C02CH2Ph l-Ethyl-3-phenyl p-toluenesulfonate l-(2-Dimethylaminoethyl)-2,3-diphenyl chloride hydrochloride Hemiethanolate... [Pg.258]

Thallic chloride. Diphenylchlorobismuthme and thallium diphenyl chloride Goddard, ibid., 1922,121, 36. [Pg.265]

STUDY OF THE THERMAL VARIATION OF THE VISCOSITY OF DIPHENYL CHLORIDES. [Pg.199]


See other pages where 3,5-diphenyl- -chloride is mentioned: [Pg.48]    [Pg.915]    [Pg.1022]    [Pg.1087]    [Pg.1091]    [Pg.973]    [Pg.974]    [Pg.975]    [Pg.975]    [Pg.975]    [Pg.975]    [Pg.975]    [Pg.977]    [Pg.1106]    [Pg.1107]    [Pg.1119]    [Pg.227]    [Pg.242]    [Pg.404]    [Pg.165]    [Pg.258]    [Pg.258]   
See also in sourсe #XX -- [ Pg.785 ]

See also in sourсe #XX -- [ Pg.785 ]




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Diphenyl copper bromide/chloride

Diphenyl copper chloride

Diphenyl ether-4,4 -disulfonyl chloride

Diphenyl iron chloride

Diphenyl palladium chloride/dichloride

Diphenyl phosphane chloride

Diphenyl platinum chloride

Diphenyl rhodium chloride

Diphenyl sulfone-3,3 -disulfonyl chloride

Diphenyl- telluronium chloride

Methanesulfonyl chloride 3- -4,5-diphenyl

Phosphinic chloride, diphenyl

Phosphoryl chloride, diphenyl

Reagents for Synthesis of Organoselenium Compounds Diphenyl Diselenide and Benzeneselenenyl Chloride

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