75872-29-6 Usage
General Description
1-[(6E)-4-methyl-1-phenyl-6-(phenylimino)-1,6-dihydropyridazin-3-yl]ethanone is a chemical compound with the molecular formula C19H18N2O. It is a dihydropyridazin-3-yl derivative containing a ketone group. 1-[(6E)-4-methyl-1-phenyl-6-(phenylimino)-1,6-dihydropyridazin-3-yl]ethanone is a potential pharmacological agent and may have applications in the field of medicinal chemistry. It possesses a unique structure with both pyridazine and ketone functionalities, which may impart specific biological activities or interactions. Further research is needed to fully understand the properties and potential uses of 1-[(6E)-4-methyl-1-phenyl-6-(phenylimino)-1,6-dihydropyridazin-3-yl]ethanone.
Check Digit Verification of cas no
The CAS Registry Mumber 75872-29-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,8,7 and 2 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 75872-29:
(7*7)+(6*5)+(5*8)+(4*7)+(3*2)+(2*2)+(1*9)=166
166 % 10 = 6
So 75872-29-6 is a valid CAS Registry Number.
75872-29-6Relevant academic research and scientific papers
Cumulated Ylides, XIV - Phosphacumulene Ylides - Building Blocks for the Synthesis of Heterocyclic Compounds
Bestmann, Hans Juergen,Schmid, Guenter,Sandmeier, Dieter,Schade, Gerold,Oechsner, Helmut
, p. 1709 - 1719 (2007/10/02)
Phosphacumulene ylides 1 and acidic compounds 4 combine to give phosphoranes 5, which cyclize by an intramolecular reaction (mostly Wittig reaction) with formation of heterocycles 7.
Stickstoff- und Schwefelheterocyclen aus NH- und SH-aciden Carbonylverbindungen und Phosphacumulenyliden
Bestmann, Hans Juergen,Schmid, Guenter,Sandmeier, Dieter
, p. 2939 - 2942 (2007/10/02)
Phosphacumulenylide reagieren mit 1,2,3-Tricarbonyl-2-phenylhydrazonen zu Pyridazinderivaten, mit β-Ketoenaminen zu Pyridindionabkoemmlingen und mit α-Ketothiocarbonsaeureamiden zu Verbindungen der Dihydrothiophendion-Reihe.
