6975-08-2 Usage
Uses
Used in Organic Synthesis:
Diphenylglyoxal is used as a reagent in organic synthesis for the formation of carbon-carbon bonds through nucleophilic addition reactions. Its unique structure allows for versatile reactions, making it a valuable component in the synthesis of complex organic molecules.
Used in Pharmaceutical and Agrochemical Synthesis:
Diphenylglyoxal serves as a building block in the synthesis of various pharmaceuticals and agrochemicals. Its ability to form carbon-carbon bonds and its compatibility with a range of chemical reactions make it a useful intermediate in the development of new drugs and agricultural chemicals.
Used in Biological Research:
Diphenylglyoxal has been studied for its potential biological activities, such as antioxidant and anti-inflammatory properties. These studies aim to explore its potential use in the development of therapeutic agents for various diseases and conditions.
Used in Antioxidant Applications:
Diphenylglyoxal is used as an antioxidant, which helps protect cells from damage caused by reactive oxygen species. Its antioxidant properties make it a candidate for use in the development of treatments for oxidative stress-related diseases.
Used in Anti-inflammatory Applications:
Diphenylglyoxal is also used for its anti-inflammatory properties, which can help reduce inflammation and alleviate symptoms associated with inflammatory conditions. This makes it a potential candidate for the development of anti-inflammatory drugs.
Check Digit Verification of cas no
The CAS Registry Mumber 6975-08-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,7 and 5 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6975-08:
(6*6)+(5*9)+(4*7)+(3*5)+(2*0)+(1*8)=132
132 % 10 = 2
So 6975-08-2 is a valid CAS Registry Number.
6975-08-2Relevant academic research and scientific papers
Lithiation and reactions of stilbene oxides: Synthetic utility
Florio, Saverio,Aggarwal, Varinder,Salomone, Antonio
, p. 4191 - 4194 (2007/10/03)
(Chemical Equation Presented) The lithiation of trans- and cis-stilbene oxides (±)-1 and 8 has been investigated. While with 8, lithiation occurred exclusively at the benzylic position, with the trans isomer (±)-1, ortho-lithiation competed with α-lithiation depending upon the experimental conditions. The configurational stability of the α-lithiated cis- and trans-stilbene oxides (±)-2 and (±)-9, respectively, was proved as well as that of scalemic stilbene oxide (R,R)-2.
