26708-04-3 Usage
Description
2-Ethyl-9,10-dimethoxyanthracene is an organic compound with potential applications in various fields due to its unique chemical properties. It is known for its antihistaminic activity and ability to participate in photoinduced electron transfer processes.
Uses
Used in Photopolymerization:
2-Ethyl-9,10-dimethoxyanthracene is used as a photosensitizer to accelerate the photopolymerization process. Its role in this application is to enhance the polymerization of benzothiazolium salts, which can be crucial for improving the efficiency and speed of certain chemical reactions in the polymer industry.
Used in Pharmaceutical Applications:
Although not explicitly mentioned in the provided materials, the antihistaminic activity of 2-Ethyl-9,10-dimethoxyanthracene suggests potential use in the development of pharmaceuticals targeting histamine-related conditions, such as allergies or asthma. Its ability to participate in photoinduced electron transfer processes could also be harnessed for various applications in drug design and delivery systems.
Used in Chemical Research:
The reported photoinduced electron transfer from the singlet excited state of 2-Ethyl-9,10-dimethoxyanthracene to CCl4 and the photosensitized reductions of 4-cyanobenzylmethylphenyl sulfonium tetrafluoroborate by its excited singlet state indicate its potential use in chemical research. These properties could be valuable for studying electron transfer processes and developing new chemical reactions or methodologies.
Check Digit Verification of cas no
The CAS Registry Mumber 26708-04-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,7,0 and 8 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 26708-04:
(7*2)+(6*6)+(5*7)+(4*0)+(3*8)+(2*0)+(1*4)=113
113 % 10 = 3
So 26708-04-3 is a valid CAS Registry Number.
InChI:InChI=1/C18H18O2/c1-4-12-9-10-15-16(11-12)18(20-3)14-8-6-5-7-13(14)17(15)19-2/h5-11H,4H2,1-3H3
26708-04-3Relevant articles and documents
Direct Synthesis of Hydroquinones from Quinones through Sequential and Continuous-Flow Hydrogenation-Derivatization Using Heterogeneous Au–Pt Nanoparticles as Catalysts
Miyamura, Hiroyuki,Tobita, Fumiya,Suzuki, Aya,Kobayashi, Shū
, p. 9220 - 9224 (2019/06/13)
Pt–Au bimetallic nanoparticle catalysts immobilized on dimethyl polysilane (Pt–Au/(DMPSi-Al2O3)) have been developed for selective hydrogenation of quinones to hydroquinones. High reactivity, selectivity, and robustness of the catalysts were confirmed under continuous-flow conditions. Various direct derivatizations of quinones, such as methylation, acetylation, trifluoromethanesulfonylation, methacrylation, and benzoylation were successfully performed under sequential and continuous-flow conditions to afford the desired products in good to excellent yields. Especially, air-sensitive hydroquinones, such as anthrahydroquinones and naphthohydroquinones, could be successfully generated and derivatized under closed sequential and continuous-flow conditions without decomposition.