27090-16-0 Usage
Uses
Used in Photopolymerization:
9-(9H-thioxanthen-9-ylidene)-9H-thioxanthene is used as a photoabsorber in photopolymerization reactions, facilitating the process of converting monomers into polymers using light as the energy source.
Used in Photoreactive Material Production:
This chemical compound is utilized in the production of photoreactive materials such as photoresists and photolithography, which are essential in the manufacturing of semiconductors and microelectronics.
Used in Organic Electronic Devices:
9-(9H-thioxanthen-9-ylidene)-9H-thioxanthene is being investigated for its potential applications in organic electronic devices, where its photoinitiating properties could enhance the performance of these devices.
Used in Solar Energy Conversion:
9-(9H-thioxanthen-9-ylidene)-9H-thioxanthene is also being explored for its use in dyes for solar energy conversion, where it could contribute to improving the efficiency of solar cells by aiding in the absorption of light.
Used in Anticancer and Antiviral Research:
Due to its potential anticancer and antiviral properties, 9-(9H-thioxanthen-9-ylidene)-9H-thioxanthene is under investigation for possible applications in the medical field, specifically for developing new treatments and therapies.
Check Digit Verification of cas no
The CAS Registry Mumber 27090-16-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,0,9 and 0 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 27090-16:
(7*2)+(6*7)+(5*0)+(4*9)+(3*0)+(2*1)+(1*6)=100
100 % 10 = 0
So 27090-16-0 is a valid CAS Registry Number.
27090-16-0Relevant academic research and scientific papers
Zinc-mediated reductive dimerizations of telluroxanthone and selenoxanthone. Tellurium-selenium selectivity
Levy,Agranat
, p. 6157 - 6160 (2007/10/03)
Reductive dimerizations of 9H-selenoxanthen-9-one (3) and 9H-telluroxanthen-9-one (4) (1:1) with zinc in boiling AcOH and HCl for 1 hour gave the bistricyclic ethanes 9,9'-bi(9H-selenoxanthene (10), 9,9'-bi(9H-telluroxanthene) (11) and 9-(9'H-telluroxanthen-9'-yl)-9H-selenoxanthene (12) in the ratios 21 (10):35 (11):44 (12) (in addition to 9H-selenoxanthene (13) and 9H-telluroxanthene (14)) Analogous reactions of 4 and 9H-thioxanthen-9-one (9) (1:1) and 3 and 9 (1:1) gave the corresponding bistricyclic ethanes. The reactions were chalcogen selective with a preference towards the tellurium-bridged bistricyclic ethanes. (C) 2000 Elsevier Science Ltd.
Novel reductive couplinog-rearrangement of carbonyl compounds with metal/Lewis acid under irradiation of ultrasonic wave
Sato, Ryu,Nagaoka, Takeshi,Saito, Minoru
, p. 4165 - 4168 (2007/10/02)
Novel reductive coupling-rearrangement of carbonyl compounds such as benzophenones with Al or Zn/ AlCl3 in CH3CN under irradiation of ultrasonic wave gave benzopinacolones via epoxides in good yields.
