59611-46-0 Usage
Classification
Ethyl ester
It is an ester formed by the reaction of the carboxylic acid group with ethanol.
Parent compound
1-oxo-6,7-dihydro-1H,5H-pyrido[3,2,1-ij]quinoline-2-carboxylic acid
The acid from which the ethyl ester is derived.
Biological and pharmacological activities
Potential activities
The compound may exhibit various properties such as antimicrobial, antiviral, or anticancer activity.
Application
Medicinal chemistry and pharmaceutical research
It is often used in these fields due to its potential biological and pharmacological activities.
Drug discovery and development
Target for investigation
The compound's specific structure and potential activities make it a promising candidate for further research and development.
Organic synthesis
Building block for complex molecules
The compound could be used as a starting material or intermediate in the synthesis of other complex molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 59611-46-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,6,1 and 1 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 59611-46:
(7*5)+(6*9)+(5*6)+(4*1)+(3*1)+(2*4)+(1*6)=140
140 % 10 = 0
So 59611-46-0 is a valid CAS Registry Number.
59611-46-0Relevant academic research and scientific papers
Radical cyclizations to quinolone and isoquinolone systems under oxidative and reductive conditions
Osornio, Yazmin M.,Miranda, Luis D.,Cruz-Almanza, Raymundo,Muchowski, Joseph M.
, p. 2855 - 2858 (2007/10/03)
Radical cyclizations to quinolone and isoquinolone systems under Fenton-type and n-Bu3SnH-mediated conditions are described. For N-iodoalkylquinolones, ca. 3:1 mixtures of oxidative cyclization products at C-2, and unexpectedly at C-8, were obtained under both conditions. Five- or six-membered oxidative cyclization products were obtained from N-iodoalkylisoquinolones under Fenton-type conditions, whereas n-Bu 3SnH-mediated reactions gave products of reductive cyclization in the five, six, and seven-membered series.
