86012-83-1 Usage
Uses
Used in Pharmaceutical Research:
4,6-Indole dicarboxylic acid methyl ester is used as a key intermediate in the synthesis of various pharmaceutical compounds due to its versatile chemical structure and functional groups. Its presence in the molecular framework of target drugs aids in enhancing their therapeutic effects.
Used in Organic Synthesis:
In the field of organic synthesis, 4,6-Indole dicarboxylic acid methyl ester is utilized as a valuable building block for the creation of a wide range of organic compounds. Its reactivity and structural features facilitate the development of new chemical entities with potential applications in various industries.
Used in Drug Development:
4,6-Indole dicarboxylic acid methyl ester is employed as a precursor in drug development for its antioxidant and anti-inflammatory properties. These characteristics make it suitable for the formulation of new drugs aimed at treating conditions associated with oxidative stress and inflammation.
Used in Antioxidant and Anti-Inflammatory Applications:
In the health and wellness industry, 4,6-Indole dicarboxylic acid methyl ester is used as a natural antioxidant and anti-inflammatory agent. Its ability to combat oxidative stress and reduce inflammation contributes to the development of products that promote overall health and well-being.
Each application underscores the compound's multifaceted utility in different sectors, highlighting its significance in modern scientific and industrial endeavors.
Check Digit Verification of cas no
The CAS Registry Mumber 86012-83-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,0,1 and 2 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 86012-83:
(7*8)+(6*6)+(5*0)+(4*1)+(3*2)+(2*8)+(1*3)=121
121 % 10 = 1
So 86012-83-1 is a valid CAS Registry Number.
86012-83-1Relevant academic research and scientific papers
Noland, Wayland E.,Lee, Chang Kiu,Bae, Sun Kun,Chung, Bong Yul,Hahn, Chi Sun,Kim, Keun Jae
, p. 2488 - 2491 (1983)
Vinylpyrroles having electron-withdrawing substituents react with dienophiles to give ? adducts while the furan and thiophene analogues do not.The difference in reactivity among the monoheterocycles can be explained in terms of the greater electron-releasing ability of the nitrogen atom in the pyrrole.The s-cis conformation of the (1H-pyrrol-2-yl)maleate derivatives appears to be an important factor in their undergoing the cycloaddition reaction.
