25862-14-0 Usage
Uses
Used in Organic Synthesis:
BIS(4-METHOXYPHENYL) SELENOXIDE is used as a reagent for introducing the selenoxide functionality into organic molecules. This functionality can be utilized in various chemical reactions and transformations, enhancing the versatility and reactivity of the target molecules.
Used as a Catalyst in Chemical Reactions:
BIS(4-METHOXYPHENYL) SELENOXIDE serves as a catalyst for a range of reactions, including the oxidation of sulfides to sulfoxides. Its catalytic properties enable more efficient and selective chemical processes, improving the overall yield and purity of the products.
Used in Pharmaceutical and Biological Research:
BIS(4-METHOXYPHENYL) SELENOXIDE has been studied for its potential biological and pharmacological properties, such as antioxidant and anti-inflammatory effects. These properties make it a promising candidate for the development of new drugs and therapeutic agents.
However, it is important to note that the use of BIS(4-METHOXYPHENYL) SELENOXIDE is limited by the potential toxicity of selenium compounds. Careful consideration and safety measures must be taken when handling and utilizing BIS(4-METHOXYPHENYL) SELENOXIDE in various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 25862-14-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,8,6 and 2 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 25862-14:
(7*2)+(6*5)+(5*8)+(4*6)+(3*2)+(2*1)+(1*4)=120
120 % 10 = 0
So 25862-14-0 is a valid CAS Registry Number.
InChI:InChI=1/C14H14O3Se/c1-16-11-3-7-13(8-4-11)18(15)14-9-5-12(17-2)6-10-14/h3-10H,1-2H3
25862-14-0Relevant academic research and scientific papers
Synthesis of 9-oxoselenoxanthenium and triarylselenonium hexafluorophosphates
Loskutov,Balina,Russkikh,Shelkovnikov
, p. 1093 - 1097 (2015/06/30)
The selenoxides forming 9-oxoselenoxanthenium and triaryl selenonium hexafluorophosphates via interaction with heptyl phenyl ether and anisole in the MeSO3H-P2O5 mixture followed by treatment with KPF6 have been obtained via selenoxantene-9-one and diphenyl selenide derivatives oxidation with m-chloroperoxybenzoic acid or hydrogen peroxide.
