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  2. 2,6-Dichlorobenzonitrile - Wikipedia

    en.wikipedia.org/wiki/2,6-Dichlorobenzonitrile

    2,6-Dichlorobenzonitrile (DCBN or dichlobenil) is an organic compound with the chemical formula C 6 H 3 Cl 2 CN. It is a white solid that is soluble in organic solvents. It is a white solid that is soluble in organic solvents.

  3. Chlorobenzonitrile - Wikipedia

    en.wikipedia.org/wiki/Chlorobenzonitrile

    2,6-Dichlorobenzonitrile This page was last edited on 7 January 2024, at 22:02 (UTC). Text is available under the Creative Commons Attribution-ShareAlike 4.0 ...

  4. 2-Chlorobenzonitrile - Wikipedia

    en.wikipedia.org/wiki/2-Chlorobenzonitrile

    This page was last edited on 8 September 2024, at 15:42 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.

  5. Category:Benzonitriles - Wikipedia

    en.wikipedia.org/wiki/Category:Benzonitriles

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us

  6. Dichlobenil - Wikipedia

    en.wikipedia.org/?title=Dichlobenil&redirect=no

    This page was last edited on 30 August 2013, at 07:40 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may ...

  7. Body broker - Wikipedia

    en.wikipedia.org/wiki/Body_broker

    A body broker (also non-transplant tissue banks) is a firm or an individual that buys and sells cadavers or human body parts.. Whereas the market for organ transplantation is heavily regulated in the United States, the use of cadaver parts for research, training, and other uses is not.

  8. Talk:2,6-Dichlorobenzonitrile - Wikipedia

    en.wikipedia.org/wiki/Talk:2,6-Dichlorobenzonitrile

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  9. Halex process - Wikipedia

    en.wikipedia.org/wiki/Halex_process

    2,6-dichlorobenzonitrile → 2,6-difluorobenzonitrile. The nitro groups in the above compounds can be reduced to give the corresponding aniline. For example, selective hydrogenation of 4-fluoronitrobenzene gives 4-fluoroaniline. Thus, the Halex method provides access to a host of fluoroanilines.