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  2. Methyl acrylate - Wikipedia

    en.wikipedia.org/wiki/Methyl_acrylate

    Methyl acrylate can be prepared by debromination of methyl 2,3-dibromopropanoate with zinc. [10] Methyl acrylate is formed in good yield on pyrolysis of methyl lactate in the presence of ethenone (ketene). [11] Methyl lactate is a renewable "green chemical". Another patent [12] describes the dehydration of methyl lactate over zeolites.

  3. Methylacrylate - Wikipedia

    en.wikipedia.org/wiki/Methylacrylate

    Methyl acrylate; The anion of methacrylic acid This page was last edited on 4 February 2015, at 16:22 (UTC). Text is available under the Creative Commons Attribution ...

  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. Poly(methyl acrylate) - Wikipedia

    en.wikipedia.org/wiki/Poly(methyl_acrylate)

    Poly(methyl acrylate) (PMA) is a family of organic polymers with the formula (CH 2 CHCO 2 CH 3) n. It is a synthetic acrylate polymer derived from methyl acrylate monomer. The polymers are colorless. This homopolymer is far less important than copolymers derived from methyl acrylate and other monomers.

  6. List of desk forms and types - Wikipedia

    en.wikipedia.org/wiki/List_of_desk_forms_and_types

    Armoire desk; Bargueño desk; Bench desk; Bible box; Bonheur du jour; Bureau à gradin; Bureau brisé; Bureau capucin; Bureau Mazarin; Bureau plat, see Writing table; Butler's desk; Campaign desk; Carlton house desk; Carrel desk; Cheveret desk; Computer desk; Credenza desk; Cubicle desk; Cylinder desk; Davenport desk; Desk and bench; Desk on a ...

  7. Acrylonitrile - Wikipedia

    en.wikipedia.org/wiki/Acrylonitrile

    This salt can be converted to acrylamide with treatment with base or to methyl acrylate by treatment with methanol. [5] The reaction of acrylonitrile with protic nucleophiles is a common route to a variety of specialty chemicals. The process is called cyanoethylation: YH + H 2 C=CHCN → Y−CH 2 −CH 2 CN

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