871583-23-2 Usage
Uses
Used in Medicinal Chemistry:
1H-Pyrrolo[2,3-b]pyridine-2-carboxylic acid, 4-chloro-, methyl ester is used as a building block or intermediate in the synthesis of biologically active compounds and pharmaceutical agents. Its unique structural features, including the 4-chloro substitution, may enhance the compound's reactivity and selectivity in chemical reactions, facilitating the development of novel therapeutic agents.
Used in Drug Discovery and Development:
In the pharmaceutical industry, 1H-Pyrrolo[2,3-b]pyridine-2-carboxylic acid, 4-chloro-, methyl ester is utilized for its potential to impart specific chemical and biological properties to compounds under development. Its presence in a molecule may influence pharmacokinetic and pharmacodynamic properties, such as solubility, stability, and binding affinity to target proteins or receptors. This makes it a promising candidate for the design and optimization of new drugs with improved efficacy and safety profiles.
Used in Research and Exploration:
1H-Pyrrolo[2,3-b]pyridine-2-carboxylic acid, 4-chloro-, methyl ester is employed in academic and industrial research settings to explore its potential applications in drug discovery. Its unique structural features and the possibility of further chemical modifications make it an interesting subject for studying structure-activity relationships and the development of new chemical entities with therapeutic potential.
Check Digit Verification of cas no
The CAS Registry Mumber 871583-23-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,1,5,8 and 3 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 871583-23:
(8*8)+(7*7)+(6*1)+(5*5)+(4*8)+(3*3)+(2*2)+(1*3)=192
192 % 10 = 2
So 871583-23-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H7ClN2O2/c1-14-9(13)7-4-5-6(10)2-3-11-8(5)12-7/h2-4H,1H3,(H,11,12)
871583-23-2Relevant articles and documents
The Hemetsberger-Knittel synthesis of substituted 5-, 6-, and 7-azaindoles
Roy, Patrick J.,Dufresne, Claude,Lachance, Nicolas,Leclerc, Jean-Philippe,Boisvert, Michel,Wang, Zhaoyin,Leblanc, Yves
, p. 2751 - 2757 (2007/10/03)
A series of substituted 5-, 6-, and 7-azaindoles were prepared via the Hemetsberger-Knittel reaction. In general, better yields were obtained at higher temperatures and shorter reaction times than required for the formation of the analogous indoles, and in some cases, only decomposition occurred below a minimum temperature. The resulting templates offer up to five sites for subsequent functionalization to allow a wide range of chemical diversity. Georg Thieme Verlag Stuttgart.
