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  2. Ethyl cyanohydroxyiminoacetate - Wikipedia

    en.wikipedia.org/wiki/Ethyl_cyanohydroxyiminoacetate

    Ethyl cyanohydroxyiminoacetate (oxyma) is the oxime of ethyl cyanoacetate and finds use as an additive for carbodiimides, such as dicyclohexylcarbodiimide (DCC) in peptide synthesis. It acts as a neutralizing reagent for the basicity or nucleophilicity of the DCC due to its pronounced acidity ( pKa 4.60) and suppresses base catalyzed side ...

  3. Ethyl cyanoacetate - Wikipedia

    en.wikipedia.org/wiki/Ethyl_cyanoacetate

    Ethyl cyanoacetate is an organic compound that contains a carboxylate ester and a nitrile. It is a colourless [ 1 ] liquid with a pleasant odor. This material is useful as a starting material for synthesis due to its variety of functional groups and chemical reactivity.

  4. Ethyl acetate - Wikipedia

    en.wikipedia.org/wiki/Ethyl_acetate

    Ethyl acetate (systematically ethyl ethanoate, commonly abbreviated EtOAc, ETAC or EA) is the organic compound with the formula CH 3 CO 2 CH 2 CH 3, simplified to C 4 H 8 O 2.This flammable, colorless liquid has a characteristic sweet smell (similar to pear drops) and is used in glues, nail polish removers, and the decaffeination process of tea and coffee.

  5. Ethyl acetate (data page) - Wikipedia

    en.wikipedia.org/wiki/Ethyl_acetate_(data_page)

    1 Material Safety Data Sheet. 2 Structure and properties. 3 Thermodynamic properties. ... for Ethyl Acetate/Acetic acid [3] P = 740 mmHg BP Temp. °C % by mole C 4 H ...

  6. Butyl cyanoacrylate - Wikipedia

    en.wikipedia.org/wiki/Butyl_cyanoacrylate

    NBCA in monomer form is soluble in acetone, methyl ethyl ketone, nitromethane, and methylene chloride. [4] It polymerizes rapidly in presence of ionic substances such as moisture, blood, or tissue fluids. NBCA has unique properties compared to other cyanoacrylates such as octyl cyanoacrylate or isoamyl cyanoacrylate.

  7. Cyanogen - Wikipedia

    en.wikipedia.org/wiki/Cyanogen

    Cyanogen is typically generated from cyanide compounds. One laboratory method entails thermal decomposition of mercuric cyanide: . 2 Hg(CN) 2 → (CN) 2 + Hg 2 (CN) 2 Or, one can combine solutions of copper(II) salts (such as copper(II) sulfate) with cyanides; an unstable copper(II) cyanide is formed which rapidly decomposes into copper(I) cyanide and cyanogen.