63190-58-9 Usage
General Description
2,3,6-trimethylquinazolin-4(3H)-one is a chemical compound with the molecular formula C11H11N3O. It belongs to the quinazolinone class of molecules, which are known for their diverse biological activities. The compound is characterized by a quinazoline ring structure with three methyl groups attached at the 2nd, 3rd, and 6th positions. 2,3,6-trimethylquinazolin-4(3H)-one has been studied for its potential pharmacological properties, including its role as a potential anti-cancer agent and as an inhibitor of various enzymes. Its unique structure and promising biological activities make it an interesting target for further research in the field of medicinal chemistry and drug development.
Check Digit Verification of cas no
The CAS Registry Mumber 63190-58-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,1,9 and 0 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 63190-58:
(7*6)+(6*3)+(5*1)+(4*9)+(3*0)+(2*5)+(1*8)=119
119 % 10 = 9
So 63190-58-9 is a valid CAS Registry Number.
63190-58-9Relevant articles and documents
Cp?CoIII-catalyzed formal [4+2] cycloaddition of benzamides to afford quinazolinone derivatives
Yang, Jingshu,Hu, Xiao,Liu, Zijie,Li, Xueyuan,Dong, Yi,Liu, Gang
, p. 13840 - 13843 (2019/11/21)
A Cp?CoIII-catalyzed arene C-H bond amidation/annulation of benzamides was developed to afford quinazolinone derivatives in one-pot with high yields and broad substrate scope. This method could be applied to the synthesis of quinazolinone drugs and late-stage modification of natural products.
Transition-Metal Complex-Catalyzed Reductive N-Heterocyclization: Synthesis of 4(3H)-Quinazolinone Derivatives from N-(2-Nitrobenzoyl)amides
Akazome, Motohiro,Kondo, Teruyuki,Watanabe, Yoshihisa
, p. 310 - 312 (2007/10/02)
Several ruthenium and platinum complexes smoothly catalyze the reductive N-heterocyclization of N-(2-nitrobenzoyl)amides under carbon monoxide pressure to afford the corresponding 4(3H)-quinazolinone derivatives, including some quinazolinone alkaloids, in
