83-80-7 Usage
Uses
Used in Organic Synthesis:
1,5-Dibenzoylnaphthalene is used as a reagent in organic synthesis for its capacity to undergo multiple chemical reactions, contributing to the creation of a wide range of organic compounds.
Used in Dye and Pigment Production:
As a starting material, 1,5-dibenzoylnaphthalene is utilized in the production of dyes and pigments, given its chemical properties that facilitate the development of colorants for various applications.
Used in Research and Pharmaceutical Industries:
1,5-Dibenzoylnaphthalene is employed in research and pharmaceutical industries as a starting material for the synthesis of new pharmaceutical compounds and other functional materials, owing to its reactivity and structural features that can be manipulated for specific purposes.
Check Digit Verification of cas no
The CAS Registry Mumber 83-80-7 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 8 and 3 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 83-80:
(4*8)+(3*3)+(2*8)+(1*0)=57
57 % 10 = 7
So 83-80-7 is a valid CAS Registry Number.
InChI:InChI=1/C24H16O2/c25-23(17-9-3-1-4-10-17)21-15-7-14-20-19(21)13-8-16-22(20)24(26)18-11-5-2-6-12-18/h1-16H
83-80-7Relevant articles and documents
Incorporation of the 1,5-naphthalene subunit into heteroporphyrin structure: Toward helical aceneporphyrinoids
Szyszko, Bartosz,Pacholska-Dudziak, Ewa,Latos-Grazyński, Lechos?aw
, p. 5090 - 5095 (2013)
5,10,15,20-Tetraaryl-22-hetero-1,5-naphthiporphyrins, which contain a 1,5-naphthylene moiety instead of one pyrrole embedded in the macrocyclic framework of heteroporphyrins, were obtained by the [3 + 1] approach using the 1,5-naphthylene analogue of tripyrrane (1,5-bis(phenyl(2-pyrolyl)methyl) naphthalene) and 2,5-bis(arylhydroxymethyl)heterocyclopentadiene (heterocyclopentadiene: thiophene, selenophene, tellurophene). The steric constraints, imposed by the substitution mode of the 1,5-naphthylene building block, resulted in the specific helical conformation of 22-hetero-1,5- naphthiporphyrins. The spectroscopic and structural properties of these aceneporphyrinoids indicate a lack of macrocycle aromaticity. Their protonation yielded solely dicationic species.