5369-54-0 Usage
Description
[2,2'-Bifuran]-5,5'(2H,2'H)-dione, 2,2',4,4'-tetraphenylis a chemical compound characterized by its unique structure, featuring two furan rings and four phenyl groups attached to the furan rings. This dione is a type of organic molecule that holds potential in various applications due to its distinct properties.
Uses
Used in Organic Chemistry:
[2,2'-Bifuran]-5,5'(2H,2'H)-dione, 2,2',4,4'-tetraphenylis used as a key compound in organic chemistry for its distinctive structure and properties. It serves as a valuable building block for the synthesis of other complex organic molecules, contributing to the development of novel chemical entities.
Used in Material Science:
In the field of material science, [2,2'-Bifuran]-5,5'(2H,2'H)-dione, 2,2',4,4'-tetraphenylis utilized as a component in the creation of new materials and compounds. Its unique structure allows for potential applications in various industrial sectors, enhancing the properties of materials and contributing to technological advancements.
Used in Organic Electronics:
[2,2'-Bifuran]-5,5'(2H,2'H)-dione, 2,2',4,4'-tetraphenylis employed as a component in organic electronics, where its structure and properties can be harnessed to improve the performance of electronic devices, such as organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs).
Used in Photovoltaics:
In the photovoltaic industry, [2,2'-Bifuran]-5,5'(2H,2'H)-dione, 2,2',4,4'-tetraphenylis used as a component in the development of solar cells. Its unique structure and properties can contribute to the efficiency and performance of these renewable energy technologies.
Used in Synthesis of Novel Materials:
[2,2'-Bifuran]-5,5'(2H,2'H)-dione, 2,2',4,4'-tetraphenylis also used as a starting material in the synthesis of novel materials and compounds for various industrial applications. Its structure provides a foundation for creating innovative materials with enhanced properties and potential uses in different sectors.
Check Digit Verification of cas no
The CAS Registry Mumber 5369-54-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,6 and 9 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5369-54:
(6*5)+(5*3)+(4*6)+(3*9)+(2*5)+(1*4)=110
110 % 10 = 0
So 5369-54-0 is a valid CAS Registry Number.
5369-54-0Relevant articles and documents
Photochemical and Thermal Transformations of 3-Benzyl-2(3H)-furanones and Related Substrates
Gopidas, K. R.,Cyr, D. R.,Das, P. K.,George, M. V.
, p. 5505 - 5511 (2007/10/02)
Photochemical and thermal transformations of several 2(3H)-furanones are reported.Steady-state irradiations of 3-benzyl-3,5-diphenyl-2(3H)-furanone (1a) in benzene or methanol, for example, gave a mixture of 2,3,5-triphenylfuran (3a) (8-9percent) and 1,3,5-triphenylbut-3-en-1-one (6a) (26-34percent), along with 34-37percent recovery of the unchanged starting material.Similar results were obtained with 3-benzyl-3-(4-methylphenyl)-5-phenyl-2-(3H)-furanone (1b) and 3-benzyl-3-(4-methoxyphenyl)-5-phenyl-2(3H)-furanone (1c) under analogous conditions.Upon direct irradiation, 3,3-dibenzyl-5-phenyl-2(3H)-furanone (1d), however, gave only 3-benzyl-1,4-diphenylbut-3-en-1-one (6d) (80-83percent), whereas 3-benzyl-3-phenylphenanthrofuran-2(3H)-one (1e) gave only 2,3-diphenylphenanthrofuran (3e) (15-21percent).On the other hand, 3-benzoyl-3,5-diphenyl-2(3H)-furanone (1f) gave only the bis lactone 10a (72-75percent) under direct photolysis.The bis lactones 10a-c and the rearranged 5-benzyl-3,5-diaryl-2(5H)-furanones 9a-d were the major products in the course of sensitized irradiation of 1a-d in the presence of acetophenone in benzene.The thermolysis of 1a-d also led to the formation of the rearrangement products 9a-d in high yields (60-80percent).Possible mechanisms of these various photochemical and thermal reactions are discussed in terms of singlet-mediated decarbonylation, triplet-sensitized homolysis of the benzyl-to-furanone bond and probable thermal -sigmatropic shift of the benzyl group.The laser pulse photoexcitation (337.1 nm) of benzophenone in the presence of 1a-d in benzene of acetonitrile produces the short-lived triplets of the 2(3H)-furanones (τT = 0.5-3.0 μs), which subsequently undergo bond cleavage lea ding to furanoxy radicals.The spectral and kinetic features of the triplets and the radicals are presented.
