Application of 133-37-9, New Advances in Chemical Research, May 2021.The appropriate choice of redox mediator can avoid electrode passivation and overpotential, which strongly inhibit the efficient activation of substrates in electrolysis. 133-37-9, Name is (2R,3R)-rel-2,3-Dihydroxysuccinic acid, SMILES is O=C(O)[C@H](O)[C@@H](O)C(O)=O, belongs to benzisoxazole compound. In a article, author is Orlov, V. Yu., introduce new discover of the category.
Synthesis of nitroacridinones from 2,1-benzisoxazole derivatives
Reaction of 3-aryl-2,1-benzisoxazoles with concentrated nitric acid in chloroform in one stage led to their conversion into acridinone nitro derivatives.
Application of 133-37-9, Because enzymes can increase reaction rates by enormous factors and tend to be very specific, typically producing only a single product in quantitative yield, they are the focus of active research.you can also check out more blogs about 133-37-9.
Reference:
Benzisoxazole – Wikipedia,
,Benzisoxazole – an overview | ScienceDirect Topics