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  2. N-Chlorosuccinimide - Wikipedia

    en.wikipedia.org/wiki/N-Chlorosuccinimide

    N-Chlorosuccinimide (NCS) is the organic compound with the formula C 2 H 4 (CO) 2 NCl. This white solid is used for chlorinations. [2] It is also used as a mild oxidant. [3] NCS is related to succinimide, but with N-Cl in place of N-H. The N–Cl bond is highly reactive, and NCS functions as a source of "Cl +".

  3. Succinimide - Wikipedia

    en.wikipedia.org/wiki/Succinimide

    Succinimide is an organic compound with the formula (CH 2) 2 (CO) 2 NH. This white solid is used in a variety of organic syntheses, as well as in some industrial silver plating processes. The compound is classified as a cyclic imide. It may be prepared by thermal decomposition of ammonium succinate. [4]

  4. N-Iodosuccinimide - Wikipedia

    en.wikipedia.org/wiki/N-Iodosuccinimide

    Download as PDF; Printable version; In other projects Wikimedia Commons; Wikidata item; ... (NCS) and N-bromosuccinimide (NBS) which are used for similar applications.

  5. Category:Finance formatting and function templates - Wikipedia

    en.wikipedia.org/wiki/Category:Finance...

    [[Category:Finance formatting and function templates]] to the <includeonly> section at the bottom of that page. Otherwise, add <noinclude>[[Category:Finance formatting and function templates]]</noinclude> to the end of the template code, making sure it starts on the same line as the code's last character.

  6. N-Hydroxysuccinimide - Wikipedia

    en.wikipedia.org/wiki/N-Hydroxysuccinimide

    A common way to synthesize an NHS-activated acid is to mix NHS with the desired carboxylic acid and a small amount of an organic base in an anhydrous solvent. A coupling reagent such as dicyclohexylcarbodiimide (DCC) or 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (EDC) is then added to form a highly reactive activated acid intermediate.

  7. N-Bromosuccinimide - Wikipedia

    en.wikipedia.org/wiki/N-Bromosuccinimide

    NBS is commercially available. It can also be synthesized in the laboratory. To do so, sodium hydroxide and bromine are added to an ice-water solution of succinimide. The NBS product precipitates and can be collected by filtration. [2] Crude NBS gives better yield in the Wohl–Ziegler reaction. In other cases, impure NBS (slightly yellow in ...

  8. Category:Succinimides - Wikipedia

    en.wikipedia.org/wiki/Category:Succinimides

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  9. Tetramethylsuccinonitrile - Wikipedia

    en.wikipedia.org/wiki/Tetramethylsuccinonitrile

    Tetramethylsuccinonitrile or TMSN is an organic compound with the formula (C(CH 3) 2 CN) 2, classified as a dinitrile, and a colorless and odorless solid derived from 2,2'-azobis-isobutyronitrile, a common radical initiator in the manufacture of PVC: