76292-67-6 Usage
Uses
Used in Pharmaceutical Synthesis:
Ethyl iMidazo[1,5-a]pyridine-5-carboxylate is used as a key intermediate in the synthesis of various pharmaceuticals for its potential to contribute to the development of new drugs.
Used in Organic Chemistry:
Ethyl iMidazo[1,5-a]pyridine-5-carboxylate is utilized as a building block in organic chemistry reactions, facilitating the creation of diverse organic compounds for research and industrial applications.
Used in Biological Research:
Due to its potential biological activities, Ethyl iMidazo[1,5-a]pyridine-5-carboxylate may be employed in biological research to explore its interactions with biological systems and its possible applications in medicine.
Check Digit Verification of cas no
The CAS Registry Mumber 76292-67-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,2,9 and 2 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 76292-67:
(7*7)+(6*6)+(5*2)+(4*9)+(3*2)+(2*6)+(1*7)=156
156 % 10 = 6
So 76292-67-6 is a valid CAS Registry Number.
76292-67-6Relevant academic research and scientific papers
NOVEL 5 OR 8-SUBSTITUTED IMIDAZO [1, 5-a] PYRIDINES AS INDOLEAMINE AND/OR TRYPTOPHANE 2, 3-DIOXYGENASES
-
, (2016/10/31)
Disclosed herein are 5 or 8-substituted imidazo[l,5-a]pyridines and pharmaceutical compositions comprising at least one such 5 or 8-substituted imidazo[l,5-a]pyridines, processes for the preparation thereof, and the use thereof in therapy. Disclosed herein are certain 5 or 8- substituted imidazo[l,5-a]pyridines that can be useful for inhibiting indoleamine 2,3- dioxygenase and/or tryptophane 2,3-dioxygenase and for treating diseases or disorders mediated thereby.
A DIRECT METHOD FOR THE SUBSTITUTION OF IMIDAZOPYRIDINES AT POSITION 5
Blatcher, Philip,Middlemiss, David
, p. 2195 - 2196 (2007/10/02)
3-Ethylthioimidazopyridine lithiates at carbon 5.Quenching of the anion with an electrophile followed by desulphurisation gives 5-substituted imidazopyridines.
