69601-45-2 Usage
General Description
6-Hydroxy-1-methylquinolin-2(1H)-one, also known as 6-Hydroxy-1-methyl-1,2-dihydroquinolin-2-one, is a chemical compound with the molecular formula C10H9NO2. It is a derivative of quinolin-2(1H)-one and contains a hydroxyl group and a methyl group attached to the quinoline ring structure. 6-Hydroxy-1-methylquinolin-2(1H)-one has been studied for its potential pharmacological properties, including its anti-inflammatory and antioxidant activities. It has also been investigated for its potential use in the development of new drugs and therapies. Additionally, it has been used as a building block in the synthesis of various pharmaceutical and biologically active compounds. Overall, 6-Hydroxy-1-methylquinolin-2(1H)-one is a versatile compound with potential applications in the fields of pharmacology and medicinal chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 69601-45-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,6,0 and 1 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 69601-45:
(7*6)+(6*9)+(5*6)+(4*0)+(3*1)+(2*4)+(1*5)=142
142 % 10 = 2
So 69601-45-2 is a valid CAS Registry Number.
69601-45-2Relevant articles and documents
Coumarin Derivatives Exert Anti-Lung Cancer Activity by Inhibition of Epithelial–Mesenchymal Transition and Migration in A549 Cells
Barreto, Emiliano,Bourguignon, Jean-Jacques,Dos Santos Carmo, Julianderson de Oliveira,Filho, José Maria Barbosa,Mendon?a-Junior, Francisco Jaime Bezerra,Rodarte, Renato Santos,Schmitt, Martine,Silva, Simone Lara de Omena,Souza, Tayhana Priscila Medeiros,da Silva, Camila Radelley Azevedo Costa,de Aquino, Thiago Mendon?a,de Araújo, Rodrigo Santos Aquino,de Mélo, Natália Barbosa,de Moura, Ricardo Olímpio
, (2022/01/24)
A series of coumarin derivatives and isosteres were synthesized from the reaction of triflic intermediates with phenylboronic acids, terminal alkynes, and organozinc compounds through palladium-catalyzed cross-coupling reactions. The in vitro cytotoxic ef
