153715-08-3 Usage
Uses
Used in Biomedical Engineering:
9,10-Bis(3,5-dihydroxyphenyl)anthracene is used as a component in the development of bioactive coatings for medical devices, enhancing their biocompatibility and performance.
9,10-Bis(3,5-dihydroxyphenyl)anthracene is also used in the fabrication of tissue engineering scaffolds, contributing to the structural integrity and bioactivity of these constructs.
Used in Chronic Disease Management:
9,10-Bis(3,5-dihydroxyphenyl)anthracene is used as a potential therapeutic agent in the treatment and prevention of chronic diseases such as cancer, cardiovascular disease, and neurodegenerative disorders, leveraging its antioxidant and anti-inflammatory properties to mitigate disease progression.
Used in Optoelectronic Devices:
9,10-Bis(3,5-dihydroxyphenyl)anthracene is used as a photoluminescent material in the development of organic light-emitting diodes (OLEDs) and other optoelectronic devices, taking advantage of its light-emitting capabilities to improve device performance and efficiency.
Check Digit Verification of cas no
The CAS Registry Mumber 153715-08-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,7,1 and 5 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 153715-08:
(8*1)+(7*5)+(6*3)+(5*7)+(4*1)+(3*5)+(2*0)+(1*8)=123
123 % 10 = 3
So 153715-08-3 is a valid CAS Registry Number.
InChI:InChI=1/C26H18O4/c27-17-9-15(10-18(28)13-17)25-21-5-1-2-6-22(21)26(24-8-4-3-7-23(24)25)16-11-19(29)14-20(30)12-16/h1-14,27-30H
153715-08-3Relevant articles and documents
NOVEL COMPOUND For Organic light emitting diode AND COATING COMPOSITION FOR ORGANIC LAYER COMPRISING THE SAME
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Paragraph 0137; 0138; 0151; 0152; 0157; 0158; 0165; 0166, (2020/12/29)
Provided are a compound represented by chemical formula (1) and a coating liquid composition comprising the same. The above formula (1) is as described in the description of the invention.
Catalysis by organic solids. Stereoselective Diels-Alder reactions promoted by microporous molecular crystals having an extensive hydrogen- bonded network
Endo, Ken,Koike, Takashi,Sawaki, Tomoya,Hayashida, Osamu,Masuda, Hideki,Aoyama, Yasuhiro
, p. 4117 - 4122 (2007/10/03)
Anthracenebisresorcinol derivative 1 as an organic network material shows a novel catalysis in the solid state for the acrolein-cyclohexadiene Diels-Alder reaction. The suggested mechanism involves a catalytic cycle composed of sorption of the reactants in the cavities of polycrystalline host 1, preorganized intracavity reaction, and desorption of the product. The host also promotes stereoselective intracavity reactions for alkyl acrylates and cyclohexadiene but, in this case, not in a catalytic manner. Relevance of the present system as a functional organic analog of zeolites is discussed in light of the kinetics of respective elementary processes and the effects of pulverization of the catalyst thereupon as well as X-ray crystal structures.