Application In Synthesis of 1-(tert-Butyl)-1H-pyrrole-2,5-dione. The protonation of heteroatoms in aromatic heterocycles can be divided into two categories: lone pairs of electrons are in the aromatic ring conjugated system; and lone pairs of electrons do not participate. Compound: 1-(tert-Butyl)-1H-pyrrole-2,5-dione, is researched, Molecular C8H11NO2, CAS is 4144-22-3, about Photoinduced polymerization of monofunctional maleimides and donor monomers. Author is Clark, S. C.; Doucet, G. J.; Joensson, S.; Mattson, G. A.; Hoyle, C. E..
The inherent reactivity of a maleimide/donor formulation was established by polymerizing in the presence of a photoinitiator, e.g., 2,2-dimethoxy-2-phenylacetophenone. Donors, e.g, N-vinylpyrrolidone and N-Me vinylacetamide, were polymerized with maleimides, e.g., tert-butylmaleimide (I) and 2-ethylcarbonate ethylmaleimide (II). II had a greater reactivity with the corresponding donor monomers than I.
There is still a lot of research devoted to this compound(SMILES：O=C(C=C1)N(C(C)(C)C)C1=O)Application In Synthesis of 1-(tert-Butyl)-1H-pyrrole-2,5-dione, and with the development of science, more effects of this compound(4144-22-3) can be discovered.
Reference:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics