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6-phenyl-12H-dibenzo[b,h][1,6]naphthyridin-7-one is a complex organic compound belonging to the class of naphthyridines, which are fused heterocyclic compounds. This particular compound features a dibenzo[b,h] structure, meaning it has two benzene rings fused together with a naphthyridine ring. The naphthyridine ring itself is a tricyclic system consisting of two benzene rings and one pyridine ring, with the pyridine nitrogen atom at position 6. The compound is further characterized by a phenyl group attached at position 6 and a ketone functional group at position 7. This chemical structure endows the molecule with specific electronic and steric properties, which can be relevant in various chemical and pharmaceutical applications, such as the development of new drugs or materials.

977-86-6

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977-86-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 977-86-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,7 and 7 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 977-86:
(5*9)+(4*7)+(3*7)+(2*8)+(1*6)=116
116 % 10 = 6
So 977-86-6 is a valid CAS Registry Number.

977-86-6Relevant academic research and scientific papers

Dibenzonaphthyridinones: Heterocycle-to-Heterocycle Synthetic Strategies and Photophysical Studies

Palazzo, Teresa A.,Patra, Digambara,Yang, Joung S.,El Khoury, Elsy,Appleton, Mackenzie G.,Haddadin, Makhluf J.,Tantillo, Dean J.,Kurth, Mark J.

, p. 5732 - 5735 (2015/12/11)

A heterocycle-to-heterocycle strategy is presented for the preparation of highly fluorescent and solvatochromic dibenzonaphthyridinones (DBNs) via methodology that leads to the formation of a tertiary, spiro-fused carbon center. A linear correlation between the results of photophysical experiments and time dependent density functional theory calculations was observed for the λmax of excitation for DBNs with varying electronic character.

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