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  2. IUPAC nomenclature of organic chemistry - Wikipedia

    en.wikipedia.org/wiki/IUPAC_nomenclature_of...

    Common names for ketones can be derived by naming the two alkyl or aryl groups bonded to the carbonyl group as separate words followed by the word ketone. Acetone; Acetophenone; Benzophenone; Ethyl isopropyl ketone; Diethyl ketone; The first three of the names shown above are still considered to be acceptable IUPAC names.

  3. Ethyl isopropyl ketone - Wikipedia

    en.wikipedia.org/wiki/Ethyl_isopropyl_ketone

    Ethyl isopropyl ketone (2-methyl-pentan-3-one) is an aliphatic ketone with used as a reagent in organic chemistry and as a solvent. Its fully fluorinated analog is known as Novec 1230 and is used in gaseous fire suppression .

  4. Methyl isopropyl ketone - Wikipedia

    en.wikipedia.org/wiki/Methyl_isopropyl_ketone

    3-Methyl-2-butanone (methyl isopropyl ketone, MIPK) is a ketone and solvent of minor importance. It is comparable to MEK ( Methyl ethyl ketone ), but has a lower solvency and is more expensive. [ 2 ]

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  6. Diisopropylamine - Wikipedia

    en.wikipedia.org/wiki/Diisopropylamine

    Diisopropylamine is a common amine nucleophile in organic synthesis. [4] Because it is bulky, it is a more selective nucleophile than other similar amines, such as dimethylamine.

  7. Ketone - Wikipedia

    en.wikipedia.org/wiki/Ketone

    In organic chemistry, a ketone / ˈ k iː t oʊ n / is an organic compound with the structure R−C(=O)−R', where R and R' can be a variety of carbon-containing substituents. Ketones contain a carbonyl group −C(=O)− (a carbon-oxygen double bond C=O). The simplest ketone is acetone (where R and R' is methyl), with the formula (CH 3) 2 CO ...

  8. Lithium diisopropylamide - Wikipedia

    en.wikipedia.org/wiki/Lithium_diisopropylamide

    To ensure the production of the kinetic product, a slight excess (1.1 equiv) of lithium diisopropylamide is used, and the ketone is added to the base at –78 °C. Because the ketone is quickly and quantitatively converted to the enolate and base is present in excess at all times, the ketone is unable to act as a proton shuttle to catalyze the ...

  9. Diisopropyl azodicarboxylate - Wikipedia

    en.wikipedia.org/wiki/Diisopropyl_azodicarboxylate

    Diisopropyl azodicarboxylate (DIAD) is the diisopropyl ester of azodicarboxylic acid. It is used as a reagent in the production of many organic compounds . It is often used with triphenylphosphine in the Mitsunobu reaction , [ 2 ] wherein it serves as a hydride acceptor.