The Shocking Revelation of 3-Ethyl-4-methyl-2,5-dihydro-1H-pyrrol-2-one

The potential utility of systematic synthetic strategy will be applicable to efficient generations of chemical libraries of compounds to find ‘hit’ molecules. In my other articles, you can also check out more blogs about 766-36-9. Product Details of 766-36-9.

Chemical Research Letters, May 2021. The appropriate choice of redox mediator can avoid electrode passivation and overpotential, which strongly inhibit the efficient activation of substrates in electrolysis. Product Details of 766-36-9,766-36-9, Name is 3-Ethyl-4-methyl-2,5-dihydro-1H-pyrrol-2-one, SMILES is O=C1NCC(C)=C1CC, belongs to pyrrolines compound. In a document, author is Bosch, J, introduce the new discover.

Synthesis and biological evaluation of 1,3,4-triaryl-3-pyrrolin-2-ones, a new class of selective cyclooxygenase-2 inhibitors

The synthesis and structure-activity relationships (SAR) of a series of novel selective COX-2 inhibitors are reported. The results show that some of the 1,3,4-triaryl-3-pyrrolin-2-ones 1 are more potent as COX-2 inhibitors than celecoxib, and that lactam 1d has the same selectivity. (C) 2000 Elsevier Science Ltd. All rights reserved.

The potential utility of systematic synthetic strategy will be applicable to efficient generations of chemical libraries of compounds to find ‘hit’ molecules. In my other articles, you can also check out more blogs about 766-36-9. Product Details of 766-36-9.

Reference:
Pyrroline – Wikipedia,
,1-Pyrroline | C4H7N – PubChem