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  2. 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.

  3. Cyanoacetic acid - Wikipedia

    en.wikipedia.org/wiki/Cyanoacetic_acid

    In its largest scale application, cyanoacetic acid is first esterified to give ethyl cyanoacetate. Condensation of that ester with formaldehyde gives ethyl cyanoacrylate , which used as superglue. As of 2007, more than 10,000 tons of cyanoacetic acid were produced annually.

  4. Acid dissociation constant - Wikipedia

    en.wikipedia.org/wiki/Acid_dissociation_constant

    Nitric acid, with a pK value of around −1.7, behaves as a strong acid in aqueous solutions with a pH greater than 1. [23] At lower pH values it behaves as a weak acid. pK a values for strong acids have been estimated by theoretical means. [24] For example, the pK a value of aqueous HCl has been estimated as −9.3.

  5. 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 ...

  6. Ethyl cyanoacrylate - Wikipedia

    en.wikipedia.org/wiki/Ethyl_cyanoacrylate

    Ethyl cyanoacrylate (ECA), a cyanoacrylate ester, is an ethyl ester of 2-cyano-acrylic acid. It is a colorless liquid with low viscosity and a faint sweet smell in pure form. It is the main component of cyanoacrylate glues and can be encountered under many trade names . [ 2 ]

  7. Cyanoacetamide - Wikipedia

    en.wikipedia.org/wiki/Cyanoacetamide

    This article about an organic compound is a stub. You can help Wikipedia by expanding it.

  8. Protein pKa calculations - Wikipedia

    en.wikipedia.org/wiki/Protein_pKa_calculations

    See Amino acid for the pK a values of all amino acid side chains inferred in such a way. There are also numerous experimental studies that have yielded such values, for example by use of NMR spectroscopy. The table below lists the model pK a values that are often used in a protein pK a calculation, and contains a third column based on protein ...

  9. Ethyl acetate (data page) - Wikipedia

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

    J H-H (in ethyl), 7.1 Hz. MS; Masses of main fragments 88.0 (5.1%), 70.0 (9.9%), 61.0 (14.9%), 45.0 (14.7%), 43.0 (100.0%), 29.0 (13.7%) References a b c ...