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(R)-Methyl 2-(2-chlorobenzylamino)-1-(2,3-dihydro-1H-inden-1-yl)-1H-imidazo[4,5-b]pyridine-5-carboxylate is a complex organic compound that features a methyl group, a chlorobenzylamino group, a dihydro-1H-inden-1-yl group, and an imidazo[4,5-b]pyridine-5-carboxylate group. As a carboxylate ester, it possesses a carboxylic acid functional group that has been esterified with a methyl group. (R)-Methyl 2-(2-chlorobenzylaMino)-1-(2,3-dihydro-1H-inden-1-yl)-1H-iMidazo[4,5-b]pyridine-5-carboxylate holds potential for pharmaceutical or research applications, with its specific uses and properties contingent upon its precise structure and behavior.

1426654-48-9

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1426654-48-9 Usage

Uses

Used in Pharmaceutical Industry:
(R)-Methyl 2-(2-chlorobenzylamino)-1-(2,3-dihydro-1H-inden-1-yl)-1H-imidazo[4,5-b]pyridine-5-carboxylate is used as a potential therapeutic agent for various medical conditions due to its complex structure and the presence of functional groups that may interact with biological targets.
Used in Research Applications:
In the field of research, (R)-Methyl 2-(2-chlorobenzylamino)-1-(2,3-dihydro-1H-inden-1-yl)-1H-imidazo[4,5-b]pyridine-5-carboxylate serves as a valuable compound for studying its interactions with different biological molecules, potentially leading to the discovery of new mechanisms of action or the development of novel drugs.

Check Digit Verification of cas no

The CAS Registry Mumber 1426654-48-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,6,6,5 and 4 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1426654-48:
(9*1)+(8*4)+(7*2)+(6*6)+(5*6)+(4*5)+(3*4)+(2*4)+(1*8)=169
169 % 10 = 9
So 1426654-48-9 is a valid CAS Registry Number.

1426654-48-9Downstream Products

1426654-48-9Relevant academic research and scientific papers

Discovery and optimization of antibacterial AccC inhibitors

Cheng, Cliff C.,Shipps Jr., Gerald W.,Yang, Zhiwei,Sun, Binyuan,Kawahata, Noriyuki,Soucy, Kyle A.,Soriano, Aileen,Orth, Peter,Xiao, Li,Mann, Paul,Black, Todd

scheme or table, p. 6507 - 6514 (2010/05/17)

The biotin carboxylase (AccC) is part of the multi-component bacterial acetyl coenzyme-A carboxylase (ACCase) and is essential for pathogen survival. We describe herein the affinity optimization of an initial hit to give 2-(2-chlorobenzylamino)-1-(cyclohe

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