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(E)-3-benzylideneimidazo[1,2-a]pyridin-2(3H)-one is a complex organic compound belonging to the class of imidazo[1,2-a]pyridines. It features a pyridine ring fused to an imidazole ring, with a benzylidene group attached to the 3-position of the imidazole. (E)-3-benzylideneimidazo[1,2-a]pyridin-2(3H)-one is characterized by its unique molecular structure, which consists of a double bond (E-configuration) between the benzylidene group and the imidazole ring. It has a molecular formula of C14H9N3O and a molecular weight of 233.24 g/mol. This chemical is of interest in the field of organic chemistry and may have potential applications in the development of pharmaceuticals or other chemical products due to its specific structural features.

6455-92-1

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6455-92-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6455-92-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,5 and 5 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6455-92:
(6*6)+(5*4)+(4*5)+(3*5)+(2*9)+(1*2)=111
111 % 10 = 1
So 6455-92-1 is a valid CAS Registry Number.

6455-92-1Downstream Products

6455-92-1Relevant academic research and scientific papers

Room-temperature phosphorescence in solution and in solid state from purely organic dyes

Yong, Guoping,She, Wenlong,Zhang, Yiman

, p. 161 - 167 (2012)

Phosphorescence has seldom been observed in purely organic dyes in the solution at room temperature. We herein report efficient phosphorescence in the solution from (E)-3-benzylideneimidazo[1,2-a]pyridin-2(3H)-one and its derivatives. This opens up a new

Stacking-induced diamagnetic/paramagnetic conversion of imidazo[1,2-a]pyridin-2(3 H)-one derivatives: Near-infrared absorption and magnetic properties in the solid state

Yong, Guoping,Zhang, Xuerui,Zhao, Yumei,She, Wenlong

, p. 2182 - 2188 (2013)

Herein, we present three imidazo[1,2-a]pyridin-2(3 H)-one derivatives that are diamagnetic in solution, but paramagnetic in the solid state, possibly owing to a stacking-induced formation of phenoxide-type radicals. Notably, a larger bathochromic shift of the absorption (even up to the near- infrared region) of these three compounds was observed in the solid state than in solution, which was attributable to the ordered columnar stacking arrangements or their single-electron character as radicals in the solid state. Interestingly, compared to that in solution, (E)-3-(pyridin-4′-ylmethylene)imidazo[1,2-a] pyridine 2(3 H)-one displayed a largely red-shifted emission (centered at 660 nm, with tailing above 800 nm) in the solid state. A larger bathochromic shift (260 nm) of the emission is an indication of better order and tight stacking in the solid state, which is brought about by the rigid and polar acceptor. These three compounds also reveal different magnetic susceptibilities at 300 K, thus implying that they possess various columnar stacking structures. Most interestingly, these three radicals exhibit unusual ferromagnetic-to- antiferromagnetic phase transitions, which can be attributed to anisotropic contraction and non-uniform slippage of the columnar stacking chains. Stacking the deck: Three organic compounds are diamagnetic in solution but paramagnetic in the solid state. These compounds also show stacking-induced NIR absorption and peculiar ferromagnetic-to-antiferromagnetic phase transition in the solid state. Copyright

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