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  2. Benzotrichloride - Wikipedia

    en.wikipedia.org/wiki/Benzotrichloride

    Benzotrichloride (BTC), also known as α,α,α-trichlorotoluene, phenyl chloroform or (trichloromethyl)benzene, is an organic compound with the formula C 6 H 5 CCl 3. Benzotrichloride is an unstable, colorless or somewhat yellowish, viscous, chlorinated hydrocarbon with a penetrating odor.

  3. 1,3,5-Trichlorobenzene - Wikipedia

    en.wikipedia.org/wiki/1,3,5-Trichlorobenzene

    1,3,5-Trichlorobenzene is an organochlorine compound.It is one of the three isomers of trichlorobenzene.Being more symmetrical than the other isomers, it exists as colourless crystals whereas the other isomers are liquids at room temperature.

  4. 1,2,3-Trichlorobenzene - Wikipedia

    en.wikipedia.org/wiki/1,2,3-Trichlorobenzene

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  5. Chlorobenzene - Wikipedia

    en.wikipedia.org/wiki/Chlorobenzene

    Chlorobenzene (abbreviated PhCl) is an aryl chloride and the simplest of the chlorobenzenes, consisting of a benzene ring substituted with one chlorine atom. Its chemical formula is C 6 H 5 Cl. This colorless, flammable liquid is a common solvent and a widely used intermediate in the manufacture of other chemicals.

  6. 2,4-Dinitrochlorobenzene - Wikipedia

    en.wikipedia.org/wiki/2,4-Dinitrochlorobenzene

    DNCB is produced commercially by the nitration of p-nitrochlorobenzene with a mixture of nitric and sulfuric acids.Other methods afford the compound less efficiently include the chlorination of 1,3-dinitrobenzene, nitration of o-nitrochlorobenzene and the dinitration of chlorobenzene.

  7. 2,3,7,8-Tetrachlorodibenzodioxin - Wikipedia

    en.wikipedia.org/wiki/2,3,7,8-Tetrachlorodibenzo...

    TCDD and dioxin-like compounds act via a specific receptor present in all cells: the aryl hydrocarbon (AH) receptor. [6] [7] [8] This receptor is a transcription factor which is involved in the expression of genes; it has been shown that high doses of TCDD either increase or decrease the expression of several hundred genes in rats. [9]

  8. Tetrachlorobenzene - Wikipedia

    en.wikipedia.org/wiki/Tetrachlorobenzene

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  9. 3-Nitrochlorobenzene - Wikipedia

    en.wikipedia.org/wiki/3-Nitrochlorobenzene

    Unlike the other isomers of nitrochlorobenzene, the meta isomer is not activated to nucleophilic substitution at the chlorine center. [1] However, 3-nitrochlorobenzene has other interesting reactivity. 3-Nitrochlorobenzene can be reduced to 3-chloroaniline with Fe/HCl mixture, the Bechamp reduction.