627511-05-1 Usage
Description
2-(4-BROMOPHENYL)-1H-PYRROLO[2,3-C]PYRIDINE is a pyrrole-containing heterocycle that is a fused tricyclic compound consisting of a pyrrole ring fused to a pyridine ring, with a 4-bromophenyl group attached to the pyrrole ring at the 2-position. It has potential applications in medicinal chemistry and drug discovery due to its unique structural and chemical properties.
Uses
Used in Medicinal Chemistry:
2-(4-BROMOPHENYL)-1H-PYRROLO[2,3-C]PYRIDINE is used as a building block in the synthesis of pharmaceuticals and biologically active molecules, as pyrrole-containing compounds often exhibit biological activity.
Used in Drug Discovery:
2-(4-BROMOPHENYL)-1H-PYRROLO[2,3-C]PYRIDINE is used as a valuable compound for research and development in drug discovery, due to its potential applications in medicinal chemistry.
Used in Organic Synthesis:
2-(4-BROMOPHENYL)-1H-PYRROLO[2,3-C]PYRIDINE is used as a valuable compound for further research and development in organic synthesis, due to its unique structural and chemical properties.
Used in Material Science:
2-(4-BROMOPHENYL)-1H-PYRROLO[2,3-C]PYRIDINE is used as a valuable compound for research and development in material science, due to its unique structural and chemical properties.
Check Digit Verification of cas no
The CAS Registry Mumber 627511-05-1 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 5 respectively.
Calculate Digit Verification of CAS Registry Number 627511-05:
(8*6)+(7*2)+(6*7)+(5*5)+(4*1)+(3*1)+(2*0)+(1*5)=141
141 % 10 = 1
So 627511-05-1 is a valid CAS Registry Number.
InChI:InChI=1/C13H9BrN2/c14-11-3-1-9(2-4-11)12-7-10-5-6-15-8-13(10)16-12/h1-8,16H
627511-05-1Relevant 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.
