10504-99-1 Usage
Uses
Used in Chemical Synthesis and Research:
Benzene,1,1'-selenonylbisis used as a reagent in chemical synthesis and research for its unique properties in organoselenium chemistry. It aids in the development of new compounds and contributes to the advancement of scientific understanding in this field.
Used in Pharmaceutical Research:
Benzene,1,1'-selenonylbisis studied for its potential applications in medicine, particularly for its antioxidant and anti-inflammatory properties. These properties make it a promising candidate for the development of new pharmaceuticals to treat various diseases and conditions.
Used in Antioxidant and Anti-inflammatory Applications:
Due to its antioxidant and anti-inflammatory properties, Benzene,1,1'-selenonylbisis being researched for its potential use in the development of treatments for conditions that involve oxidative stress and inflammation.
However, it is important to note that due to its toxic and potentially carcinogenic nature, Benzene,1,1'-selenonylbisshould be handled with caution and used only in controlled environments by trained professionals.
Check Digit Verification of cas no
The CAS Registry Mumber 10504-99-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,5,0 and 4 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 10504-99:
(7*1)+(6*0)+(5*5)+(4*0)+(3*4)+(2*9)+(1*9)=71
71 % 10 = 1
So 10504-99-1 is a valid CAS Registry Number.
10504-99-1Relevant academic research and scientific papers
Sofikiti, Nikoletta,Rabalakos, Constantinos,Stratakis, Manolis
, p. 1335 - 1337 (2004)
Aryl selenides and selenoxides trap efficiently the intermediates in the reaction of singlet oxygen with sulfides. In the co-photooxygenation of 1equiv of an aryl selenoxide with 1.3equiv of dimethyl sulfide, the aryl selenone is formed quantitatively. Ar
A general and efficient method to convert selenides into selenones by using HOF·CH3CN
Potash, Shay,Rozen, Shlomo
, p. 5574 - 5579 (2013/09/12)
A general route for the preparation of selenones (R2SeO 2) is presented. This task is achieved through the quick and high-yielding reaction of selenides (R2Se) with HOF·CH 3CN. The reaction tolerates some elusiv
Rapid oxidation of selenides, selenoxides, tellurides, and telluroxides with aqueous sodium hypochlorite
Khurana, Jitender M.,Kandpal, Bhaskar M.,Chauhan, Yogendra K.
, p. 1369 - 1375 (2007/10/03)
A simple and convenient procedure for the rapid oxidation of a variety of selenides, selenoxides, tellurides, and telluroxides with aqueous sodium hypochlorite to selenones and tellurones, respectively, has been reported in dimethylformamide at ambient te
