Safety of 2-(2-Aminoacetamido)acetic acid, New research progress on 556-50-3 in 2021.The appropriate choice of redox mediator can avoid electrode passivation and overpotential, which strongly inhibit the efficient activation of substrates in electrolysis. 556-50-3, Name is 2-(2-Aminoacetamido)acetic acid, SMILES is O=C(O)CNC(CN)=O, belongs to pyrrolines compound. In a article, author is Lerche, H, introduce new discover of the category.
Maillard reaction of D-glucose: Identification of a colored product with hydroxypyrrole and hydroxypyrrolinone rings connected by a methine group
Investigation of the colored products formed by the reaction Of D-glucose with butylammoniurn acetate has been extended. The previously unknown 1-N-butyl-4-hydroxy-5-methyl-2-(N-butyl-3-hydroxy-5-(2-hydroxyethyl)pyrrolyl-2-methylidene)-2H-pyrrolin-3-one (2a) was isolated from the reaction mixture and identified after acylation by spectroscopic data. Butylaminammonium acetate was used as a model compound representing the lysine side chains of proteins.
Safety of 2-(2-Aminoacetamido)acetic acid, This is the end of this tutorial post, and I hope it has helped your research about 556-50-3.
Reference:
Pyrroline – Wikipedia,
,1-Pyrroline | C4H7N – PubChem