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Phenanthro[9,10-g]pteridine-11,13(10H,12H)-dione is a complex organic compound belonging to the class of pteridines, which are heterocyclic compounds with a pyrimido[4,5-b]indole structure. This specific compound features a phenanthrene moiety fused to the pteridine core, with two carbonyl groups at positions 11 and 13, and two hydrogen atoms at positions 10 and 12. It is characterized by its unique molecular structure and potential applications in various fields, such as pharmaceuticals and materials science. The compound's properties, reactivity, and potential uses are determined by its molecular structure, which includes the presence of aromatic rings, nitrogen atoms, and functional groups.

5768-84-3

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5768-84-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5768-84-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,6 and 8 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5768-84:
(6*5)+(5*7)+(4*6)+(3*8)+(2*8)+(1*4)=133
133 % 10 = 3
So 5768-84-3 is a valid CAS Registry Number.

5768-84-3Downstream Products

5768-84-3Relevant academic research and scientific papers

Novel riboflavin-inspired conjugated bio-organic semiconductors

Richtar, Jan,Heinrichova, Patricie,Apaydin, Dogukan Hazar,Schmiedova, Veronika,Yumusak, Cigdem,Kovalenko, Alexander,Weiter, Martin,Sariciftci, Niyazi Serdar,Krajcovic, Jozef

, (2018/09/12)

Flavins are known to be extremely versatile, thus enabling routes to innumerable modifications in order to obtain desired properties. Thus, in the present paper, the group of bio-inspired conjugated materials based on the alloxazine core is synthetized using two efficient novel synthetic approaches providing relatively high reaction yields. The comprehensive characterization of the materials, in order to evaluate the properties and application potential, has shown that the modification of the initial alloxazine core with aromatic substituents allows fine tuning of the optical bandgap, position of electronic orbitals, absorption and emission properties. Interestingly, the compounds possess multichromophoric behavior, which is assumed to be the results of an intramolecular proton transfer.

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