Liu, Fangyao published the artcileControlled radical polymerization of N-acryloylglycinamide and UCST-type phase transition of the polymers, Name: N-(2-Amino-2-oxoethyl)acrylamide, the publication is Journal of Polymer Science, Part A: Polymer Chemistry (2012), 50(23), 4920-4928, database is CAplus.
N-Acryloylglycinamide was polymerized via the reversible addition fragmentation transfer process without sacrificing its key property, the upper critical solution temperature in water. This could be achieved by choosing an appropriate nonionic initiator [2,2′-azobis(4-methoxy-2.4-dimethyl valeronitrile) (V-70)] and nonionic chain-transfer agent (cyanomethyl dodecyl trithiocarbonate). A good molar mass control was accomplished as proved by the linear increase of molar mass with conversion, a chain extension experiment, and low dispersity. The influence of molar mass, polymer end groups, or salt concentration on the cloud point was analyzed by turbidimetry. Polymer end groups exerted a distinct effect on the cloud points, whereas the influence increased with decreasing molar masses. © 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2012.
Journal of Polymer Science, Part A: Polymer Chemistry published new progress about 2479-62-1. 2479-62-1 belongs to amides-buliding-blocks, auxiliary class Monomers,Acrylamide Monomers, name is N-(2-Amino-2-oxoethyl)acrylamide, and the molecular formula is C5H8N2O2, Name: N-(2-Amino-2-oxoethyl)acrylamide.
Referemce:
https://en.wikipedia.org/wiki/Amide,
Amide – an overview | ScienceDirect Topics