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[1,2,4]Triazolo[1,5-a]pyridine-7-carboxaldehyde, 2-phenyl- is a complex organic compound with the molecular formula C13H8N4O. It features a triazolo[1,5-a]pyridine core, which is a fused ring system consisting of a triazole and a pyridine. The molecule is characterized by a carboxaldehyde group at the 7-position and a phenyl group at the 2-position. [1,2,4]Triazolo[1,5-a]pyridine-7-carboxaldehyde, 2-phenyl- is of interest in organic chemistry and medicinal chemistry due to its potential applications in the synthesis of various pharmaceuticals and agrochemicals. Its unique structure allows for the formation of diverse derivatives, making it a valuable building block in the development of new compounds with specific biological activities.

65966-19-0

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65966-19-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65966-19-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,9,6 and 6 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 65966-19:
(7*6)+(6*5)+(5*9)+(4*6)+(3*6)+(2*1)+(1*9)=170
170 % 10 = 0
So 65966-19-0 is a valid CAS Registry Number.

65966-19-0Downstream Products

65966-19-0Relevant academic research and scientific papers

Synthesis and characterization of novel classes of PDE10A inhibitors - 1H-1,3-benzodiazoles and imidazo[1,2-a]pyrimidines

Moszczyński-P?tkowski, Rafa?,Majer, Jakub,Borkowska, Ma?gorzata,Bojarski, ?ukasz,Janowska, Sylwia,Mat?oka, Miko?aj,Stefaniak, Filip,Smuga, Damian,Bazyd?o, Katarzyna,Dubiel, Krzysztof,Wieczorek, Maciej

, p. 96 - 116 (2018)

New compounds containing [1,2,4]triazolo [1,5-a]pyridine (I), pyrazolo [1,5-a]pyridine (II), 1H-1,3-benzodiazole (III) and imidazo [1,2-a]pyrimidine (IV) backbones were designed and synthesized for PDE10A interaction. Among these compounds, 1H-1,3-benzodiazoles and imidazo [1,2-a]pyrimidines showed the highest affinity for PDE10A enzyme as well as good metabolic stability. Both classes of compounds were identified as selective and potent PDE10A enzyme inhibitors.

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