627511-04-0 Usage
Uses
Used in Pharmaceutical Industry:
2-(4-TRIFLUOROMETHYLPHENYL)-1H-PYRROLO[2,3-C]PYRIDINE is used as a potential candidate for drug development for the treatment of various diseases and disorders. Its unique structure and properties make it a valuable target for further research and development in the pharmaceutical industry.
Used in Medicinal Chemistry:
2-(4-TRIFLUOROMETHYLPHENYL)-1H-PYRROLO[2,3-C]PYRIDINE is used as a compound with inhibitory effects on certain enzymes and receptors, making it a promising candidate for the development of new therapeutic agents.
Used in Drug Development:
2-(4-TRIFLUOROMETHYLPHENYL)-1H-PYRROLO[2,3-C]PYRIDINE is used as a chemical entity with potential applications in the discovery and development of new drugs, given its interesting biological activities and pharmacological properties.
Check Digit Verification of cas no
The CAS Registry Mumber 627511-04-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,2,7,5,1 and 1 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 627511-04:
(8*6)+(7*2)+(6*7)+(5*5)+(4*1)+(3*1)+(2*0)+(1*4)=140
140 % 10 = 0
So 627511-04-0 is a valid CAS Registry Number.
InChI:InChI=1/C14H9F3N2/c15-14(16,17)11-3-1-9(2-4-11)12-7-10-5-6-18-8-13(10)19-12/h1-8,19H
627511-04-0Relevant articles and documents
A novel one-step synthesis of 2-substituted 6-azaindoles from 3-amino-4-picoline and carboxylic esters
Song, Jinhua J.,Tan, Zhulin,Gallou, Fabrice,Xu, Jinghua,Yee, Nathan K.,Senanayake, Chris H.
, p. 6512 - 6514 (2007/10/03)
Dilithiation of 3-amino-4-picoline (1) was achieved with sec-BuLi at room temperature. Condensation of the resulting dianion (2) with carboxylic esters afforded a wide range of 2-substituted 6-azaindoles in good yields.
Synthesis of 2-aryl-1-hydroxyazaindoles and 2-arylazaindoles via oxidation of o-hydroxyaminostyrylpyridines
Kuzmich, Daniel,Mulrooney, Carol
, p. 1671 - 1678 (2007/10/03)
2-Aryl-1-hydroxyazaindoles (pyrrolopyridin-1-ols) are prepared via an oxidation/cyclization of o-hydroxyaminostyrylpyridines with DDQ. Reduction of the N-OH bond affords the corresponding 2-arylazaindoles (1H-pyrrolopyridines). The scope of the cyclization is explored via (i) the condensation of 4-methyl-3-nitropyridine with various aryl aldehydes to afford 2-aryl substituted 6-azaindoles and, (ii) the synthesis of 2-phenyl-4-, 5- and 7-azaindoles.
