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  2. Ethyl cyanoacrylate - Wikipedia

    en.wikipedia.org/wiki/Ethyl_cyanoacrylate

    Ethyl cyanoacrylate is prepared by the condensation of formaldehyde with ethyl cyanoacetate: NCCH 2 CO 2 C 2 H 5 + CH 2 O → H 2 C=C(CN)CO 2 C 2 H 5 + H 2 O. This exothermic reaction affords the polymer, which is subsequently sintered, thermally "cracked" to give the monomer. Alternatively, it can be prepared by the ethoxycarbonylation of ...

  3. Cyanoacrylate - Wikipedia

    en.wikipedia.org/wiki/Cyanoacrylate

    Structure of the backbone of a cyanoacrylate polymer. Cyanoacrylates are a family of strong fast-acting adhesives with industrial, medical, and household uses. They are derived from ethyl cyanoacrylate and related esters. The cyanoacrylate group in the monomer rapidly polymerizes in the presence of water to form long, strong chains. [1]

  4. Acrylate - Wikipedia

    en.wikipedia.org/wiki/Acrylate

    The acrylate ion is the anion CH 2 =CHCO − 2. Often, acrylate refers to esters of acrylic acid, the most common member being methyl acrylate. These acrylates contain vinyl groups. These compounds are of interest because they are bifunctional: the vinyl group is susceptible to polymerization and the carboxylate group carries myriad ...

  5. Ethyl cyanoacetate - Wikipedia

    en.wikipedia.org/wiki/Ethyl_cyanoacetate

    Ethyl cyanoacrylate, used as superglue, via reaction with formaldehyde; Ethyl cyanoacetate is also used to prepare 3,3-diphenylpropan-1-amine, which is the precursor used in the synthesis of Prenylamine & Droprenilamine.

  6. Cyanoacetic acid - Wikipedia

    en.wikipedia.org/wiki/Cyanoacetic_acid

    [1] [2] Electrosynthesis by cathodic reduction of carbon dioxide and anodic oxidation of acetonitrile also affords cyanoacetic acid. [3] Cyanoacetic acid is used to do cyanoacetylation, first convenient method described by J. Slätt. [4] It is about 1000x more acidic than acetic acid, with a pK a of 2.5. Ka=2.8x10^-3

  7. Ethyl acrylate - Wikipedia

    en.wikipedia.org/wiki/Ethyl_acrylate

    Ethyl acrylate is an organic compound with the formula CH 2 CHCO 2 CH 2 CH 3. It is the ethyl ester of acrylic acid. It is a colourless liquid with a characteristic acrid odor. It is mainly produced for paints, textiles, and non-woven fibers. [5] It is also a reagent in the synthesis of various pharmaceutical intermediates.

  8. Acrylate polymer - Wikipedia

    en.wikipedia.org/wiki/Acrylate_polymer

    Acrylic elastomer is a general term for a type of synthetic rubber whose primary component is acrylic acid alkyl ester (ethyl or butyl ester). [3] Acrylic elastomer possesses characteristics of heat and oil resistance, with the ability to withstand temperatures of 170–180 °C. It is used primarily for producing oil seals and packaging related ...

  9. Cyanoethylation - Wikipedia

    en.wikipedia.org/wiki/Cyanoethylation

    Cyanoethylation is a process for the attachment of CH 2 CH 2 CN group to another organic substrate. The method is used in the synthesis of organic compounds. [1] Cyanoethylation entails addition of protic nucleophiles to acrylonitrile. Typical protic nucleophiles are alcohols, thiols, and amines. Two new bonds form: C-H and C-X (X = carbon ...