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  2. 2,4-Dinitrochlorobenzene - Wikipedia

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

    2,4-Dinitrochlorobenzene (DNCB) is an organic compound with the chemical formula (O 2 N) 2 C 6 H 3 Cl. It is a yellow solid that is soluble in organic solvents . It is an intermediate for the industrial production of other compounds.

  3. Hydrazines - Wikipedia

    en.wikipedia.org/wiki/Hydrazines

    [2] The reduction of benzenediazonium chloride with tin(II) chloride and hydrochloric acid provides phenylhydrazine. [2] 2,4-Dinitrophenylhydrazine is produced by the reaction of 1-chloro-2,4-dinitrobenzene with hydrazine. [2] Tetraphenylhydrazine is formed by the oxidation of diphenylamine with potassium permanganate in acetone. [2]

  4. Dinitrobenzene - Wikipedia

    en.wikipedia.org/wiki/Dinitrobenzene

    The three possible arrangements of the nitro groups afford three isomers, 1,2-dinitrobenzene, 1,3-dinitrobenzene, and 1,4-dinitrobenzene. Each isomer has the chemical formula C 6 H 4 N 2 O 4 and a molar mass of about 168.11 g/mol. 1,3-Dinitrobenzene is the most common isomer and it is used in the manufacture of explosives .

  5. Halex process - Wikipedia

    en.wikipedia.org/wiki/Halex_process

    1,4-dichloronitrobenzene → 1-chloro-4-fluoro-3-nitrobenzene 1-chloro-2,4-dinitrobenzene → 1-fluoro-2,4-dinitrobenzene 5-chloro-2-nitrobenzotrifluoride → 5-fluoro-2-nitrobenzotrifluoride 1,3-dichloro-4-nitrobenzene → 1,3-difluoro-4-nitrobenzene 2,6-dichlorobenzonitrile → 2,6-difluorobenzonitrile. The nitro groups in the above compounds ...

  6. Reduction of nitro compounds - Wikipedia

    en.wikipedia.org/wiki/Reduction_of_nitro_compounds

    The reduction of nitroaromatics is conducted on an industrial scale. [1] Many methods exist, such as: Catalytic hydrogenation using: Raney nickel [2] or palladium-on-carbon, [3] [4] [5] platinum(IV) oxide, or Urushibara nickel. [6] Iron in acidic media. [7] [8] [9] Sodium hydrosulfite [10] Sodium sulfide (or hydrogen sulfide and base ...

  7. 1,4-Dichloro-2-nitrobenzene - Wikipedia

    en.wikipedia.org/wiki/1,4-Dichloro-2-nitrobenzene

    Disperse Yellow 42, a popular dye for polyesters, is derived from 1,4-dichloro-2-nitrobenzene. [1] 1,4-Dichloro-2-nitrobenzene is an organic compound with the formula C 6 H 3 Cl 2 NO 2. One of several isomers of dichloronitrobenzene, it is a yellow solid that is insoluble in water. It is produced by nitration of 1,4-dichlorobenzene. It is a ...

  8. Dinitroaniline - Wikipedia

    en.wikipedia.org/wiki/Dinitroaniline

    2,4-Dinitroaniline can be prepared by reaction of 1-chloro-2,4-dinitrobenzene with ammonia or by acid hydrolysis of 2,4-dinitroacetanilide. [ 1 ] Dinitroanilines are explosive and flammable with heat or friction.

  9. 1,2-Dichloro-4-nitrobenzene - Wikipedia

    en.wikipedia.org/wiki/1,2-Dichloro-4-nitrobenzene

    1,2-Dichloro-4-nitrobenzene is an organic compound with the formula 1,2-Cl 2 C 6 H 3-4-NO 2. This pale yellow solid is related to 1,2-dichlorobenzene by the replacement of one H atom with a nitro functional group. This compound is an intermediate in the synthesis of agrochemicals.

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