1363380-47-5 Usage
Uses
Used in Pharmaceutical Industry:
6-Bromo-imidazo[1,5-a]pyridine-1-carboxylic acid ethyl ester is used as a building block for the synthesis of various bioactive molecules. Its heterocyclic structure allows for interactions with biological targets, making it a valuable starting material for drug discovery and development.
Used in Organic Synthesis:
6-Bromo-imidazo[1,5-a]pyridine-1-carboxylic acid ethyl ester is used as a versatile intermediate in organic synthesis due to its ethyl ester functional group. This group enables esterification reactions with other compounds, facilitating the creation of a wide range of chemical products.
Used in Anticancer Agents Development:
6-Bromo-imidazo[1,5-a]pyridine-1-carboxylic acid ethyl ester is used as a precursor in the development of potential anticancer agents. Its ability to interact with biological targets makes it a promising candidate for the creation of new cancer treatments.
Used in Antiviral Agents Development:
6-Bromo-imidazo[1,5-a]pyridine-1-carboxylic acid ethyl ester is also used as a precursor in the development of antiviral agents. Its heterocyclic nature and functional groups make it suitable for the design of molecules that can target and inhibit viral replication.
Check Digit Verification of cas no
The CAS Registry Mumber 1363380-47-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,3,3,8 and 0 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1363380-47:
(9*1)+(8*3)+(7*6)+(6*3)+(5*3)+(4*8)+(3*0)+(2*4)+(1*7)=155
155 % 10 = 5
So 1363380-47-5 is a valid CAS Registry Number.
1363380-47-5Relevant academic research and scientific papers
Mennie, Katrina M.,Reutershan, Michael H.,White, Catherine,Adams, Bruce,Becker, Bridget,Deng, James,Katz, Jason D.,Lablue, Elisabeth,Margrey, Kaila,Saurí, Josep
, p. 4694 - 4698 (2021)
Nitrogenous heterocycles are ubiquitous in pharmaceuticals and drug-like compounds; however, regioselective synthesis has proved challenging. Herein we report our efforts to develop a regioselective method for the synthesis of pyrazolo[1,5-a]pyridines and the serendipitous discovery of a protocol for the regioselective formation of imidazo[1,5-a]pyridines. Together, these transformations allow for the rapid and selective formation of two important heterocyclic motifs from a common intermediate.
