79252-84-9 Usage
Uses
Used in Medical and Pharmaceutical Fields:
1-(2-Hydroxyphenyl)-2,5-pyrrolidinedione is used as an iron chelator for treating iron overload conditions. Its ability to bind with iron ions makes it a potential therapeutic agent for managing diseases associated with excessive iron levels in the body.
Used in Antioxidant Applications:
Possessing antioxidant properties, 1-(2-Hydroxyphenyl)-2,5-pyrrolidinedione is used to protect cells from oxidative damage. Its capacity to neutralize reactive oxygen species may contribute to its utility in preventing or treating conditions caused by oxidative stress.
Further research is necessary to fully explore the potential uses and effects of 1-(2-Hydroxyphenyl)-2,5-pyrrolidinedione in various applications, ensuring its safety and efficacy in practical scenarios.
Check Digit Verification of cas no
The CAS Registry Mumber 79252-84-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,2,5 and 2 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 79252-84:
(7*7)+(6*9)+(5*2)+(4*5)+(3*2)+(2*8)+(1*4)=159
159 % 10 = 9
So 79252-84-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H9NO3/c12-8-4-2-1-3-7(8)11-9(13)5-6-10(11)14/h1-4,12H,5-6H2
79252-84-9Relevant academic research and scientific papers
Ru-Catalyzed Selective C-H Bond Hydroxylation of Cyclic Imides
Yuan, Yu-Chao,Bruneau, Christian,Dorcet, Vincent,Roisnel, Thierry,Gramage-Doria, Rafael
, p. 1898 - 1907 (2019/02/05)
We report on cyclic imides as weak directing groups for selective monohydroxylation reactions using ruthenium catalysis. Whereas acyclic amides are known to promote the hydroxylation of the C(sp2)-H bond enabling five-membered ring ruthenacycle intermediates, the cyclic imides studied herein enabled the hydroxylation of the C(sp2)-H bond via larger six-membered ruthenacycle intermediates. Furthermore, monohydroxylated products were exclusively obtained (even in the presence of overstoichiometric amounts of reagents), which was rationalized by the difficulty to accommodate coplanar intermediates once the first hydroxyl group was introduced into the substrate. The same reactivity was observed in the presence of palladium catalysts.
