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Ethyl acrylate reacts with amines catalyzed by Lewis acids in a Michael addition to β-alanine derivatives in high yields: [13]. The nucleophilic addition at ethyl acrylate as an α,β-unsaturated carbonyl compound is a frequent strategy in the synthesis of pharmaceutical intermediates.
Acrylates are defined by the formula CH 2 =CHCO 2 R, where R can be many groups: Acrylic acid; Methyl acrylate; Ethyl acrylate; 2-Chloroethyl vinyl ether; 2-Ethylhexyl acrylate; Butyl acrylate; Trimethylolpropane triacrylate (TMPTA) The versatility of the resulting polymers is owed to the range of R groups. Structures of some acrylates
2-Ethylhexyl acrylate is a colorless liquid acrylate used in the making of paints, [2] plastics [3] and adhesives. [4] It has an odor that has been variously described as pleasant [ 5 ] or acrid and musty.
Dimethylaminoethyl acrylate (2-dimethylaminoethyl acrylate) or DMAEA is an unsaturated carboxylic acid ester having a tertiary amino group. It is a colorless to yellowish, water-miscible liquid with a pungent, amine-like odor. DMAEA is an important acrylic monomer that gives basic properties to copolymers.
Poly(ethyl acrylate) (PEA) is a family of organic polymers with the formula (CH 2 CHCO 2 CH 2 CH 3) n. It is a synthetic acrylate polymer derived from ethyl acrylate monomer. The polymers are colorless. This homopolymer is far less important than copolymers derived from ethyl acrylate and other monomers.
Glycol ethers are designated "E-series" or "P-series" for those made from ethylene oxide or propylene oxide, respectively.Typically, E-series glycol ethers are found in pharmaceuticals, sunscreens, cosmetics, inks, dyes and water-based paints, while P-series glycol ethers are used in degreasers, cleaners, aerosol paints and adhesives.
2-Ethylhexyl acrylate This page was last edited on 4 November 2023, at 17:13 (UTC). Text is available under the Creative Commons Attribution-ShareAlike 4. ...
1,3-Dipolar cycloadditions experience very little solvent effect because both the reactants and the transition states are generally non-polar. For example, the rate of reaction between phenyl diazomethane and ethyl acrylate or norbornene (see scheme below) changes only slightly upon varying solvents from cyclohexane to methanol. [14]