49609-07-6 Usage
Uses
Used in Pharmaceutical Synthesis:
6-NITROQUINOLIN-2-AMINE is used as a key intermediate in the synthesis of various pharmaceuticals, contributing to the development of new drugs with diverse therapeutic applications.
Used in Agrochemical Production:
In the agrochemical industry, 6-NQA is utilized as a precursor in the production of agrochemicals, aiding in the creation of compounds designed to protect crops and enhance agricultural productivity.
Used in Anti-Cancer Drug Development:
6-NITROQUINOLIN-2-AMINE is employed as a potential anti-cancer agent, with ongoing research exploring its ability to target and inhibit the growth of cancer cells, offering new avenues for cancer treatment.
Used as a Ligand for Metal Complexes:
6-NQA serves as a ligand in the formation of metal complexes, which have applications in various fields, including catalysis, materials science, and medicinal chemistry.
Used in Fluorescence Probe Development:
6-NITROQUINOLIN-2-AMINE is used as a potential fluorescence probe, leveraging its optical properties to detect and monitor biological processes, with implications for diagnostics and research.
Check Digit Verification of cas no
The CAS Registry Mumber 49609-07-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,9,6,0 and 9 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 49609-07:
(7*4)+(6*9)+(5*6)+(4*0)+(3*9)+(2*0)+(1*7)=146
146 % 10 = 6
So 49609-07-6 is a valid CAS Registry Number.
49609-07-6Relevant articles and documents
2-Aminoquinoline melanin-concentrating hormone (MCH)1R antagonists
Jiang, Jinlong,Hoang, Myle,Young, Jonathan R.,Chaung, Danny,Eid, Ronsar,Turner, Cherilyn,Lin, Peter,Tong, Xinchun,Wang, Junying,Tan, Carina,Feighner, Scott,Palyha, Oksana,Hreniuk, Donna L.,Pan, Jie,Sailer, Andreas W.,MacNeil, Douglas J.,Howard, Andrew,Shearman, Lauren,Stribling, Sloan,Camacho, Ramon,Strack, Alison,Van der Ploeg, Lex H.T.,Goulet, Mark T.,DeVita, Robert J.
, p. 5270 - 5274 (2007/10/03)
A series of 2-aminoquinoline compounds was prepared and evaluated in MCH1R binding and functional antagonist assays. Small dialkyl, methylalkyl, methylcycloalkyl, and cyclic amines were tolerated at the quinoline 2-position. The in vivo efficacy of compound 12 was explored and compared to that of a related inactive analog to determine their effects on food intake and body weight in rodents.
Cyclocondensation of 2-fluoro-5-nitrobenzaldehyde with amidines. New synthesis of isoquinolines
Dar'in,Selivanov,Lobanov,Potekhin
, p. 888 - 894 (2007/10/03)
The direction of the cyclocondensation of 2-fluoro-5-nitrobenzaldehyde with five amidines having α-hydrogen atoms has been studied. It was established that depending on the structure of the amidine the main products of the reaction may be not only quinazo
