727652-08-6 Usage
General Description
2-(4-Bromo-phenyl)-7-methyl-imidazo[1,2-a]pyridine-3-carbaldehyde is a chemical compound with the molecular formula C14H10BrN3O. It is a heterocyclic compound containing an imidazo[1,2-a]pyridine core with a 4-bromo-phenyl group and a 7-methyl group attached. The compound also contains a carbaldehyde functional group attached to the third carbon of the imidazo[1,2-a]pyridine ring. This chemical compound may have potential applications in various fields such as pharmaceuticals, agrochemicals, and materials science, due to its diverse chemical structure and potential reactivity. Further research and testing may be necessary to fully understand the properties and potential uses of 2-(4-BROMO-PHENYL)-7-METHYL-IMIDAZO[1,2-A]PYRIDINE-3-CARBALDEHYDE.
Check Digit Verification of cas no
The CAS Registry Mumber 727652-08-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,2,7,6,5 and 2 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 727652-08:
(8*7)+(7*2)+(6*7)+(5*6)+(4*5)+(3*2)+(2*0)+(1*8)=176
176 % 10 = 6
So 727652-08-6 is a valid CAS Registry Number.
727652-08-6Relevant academic research and scientific papers
Synthesis and antimicrobial activity of novel imidazo[1,2-a]pyridinopyrimidine-2,4,6(1H,3H,5H)-triones and thioxopyrimidine-4,6(1H,5H)diones
Rajitha,Ravibabu,Ramesh,Rajitha
, p. 1989 - 1998 (2016/03/16)
A novel series of imidazo[1,2-a]pyridinopyrimidine-2,4,6(1H,3H,5H)-triones and thioxopyrimidine-4,6(1H,5H)diones were synthesized via multistep synthesis starting from 2-aminopyridine on cyclisation with phenacyl bromide followed by Vilsmeier-Haack and Kn
One-pot multicomponent synthesis of novel substituted imidazo[1,2-a]pyridine incorporated thiazolyl coumarins and their antimicrobial activity
Gali, Rajitha,Banothu, Janardhan,Bavantula, Rajitha
, p. 641 - 646 (2015/05/13)
A series of novel substituted imidazo[1,2-a]pyridine incorporated thiazolyl coumarin derivatives (4a, 4b, 4c, 4d, 4e, 4f, 4g, 4h, 4i, 4j, 4k, 4l, 4m, 4n, 4o, 4p, 4q, 4r, 4s, 4t) were synthesized in good yields via one-pot multicomponent condensation of su
