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  2. 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 .

  3. 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.

  4. 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 ...

  5. 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 ]

  6. 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 ...

  7. QL (chemical) - Wikipedia

    en.wikipedia.org/wiki/QL_(chemical)

    This page was last edited on 20 December 2024, at 07:13 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.

  8. N,N-Diisopropylaminoethanol - Wikipedia

    en.wikipedia.org/wiki/N,N-Diisopropylaminoethanol

    Inhalation and skin contact are expected to be the primary ways of occupational exposure to this chemical. Based on single exposure animal tests, it is considered to be slightly toxic if swallowed or inhaled, moderately toxic if absorbed through skin as well as being corrosive to eyes and skin. [1]

  9. 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.