6339-47-5 Usage
Class of Compound
Organic compounds, specifically indoles.
Structure
Unique structure containing a butane-1,4-dione and diphenyl group, as well as the indole moiety.
Pharmaceutical Potential
Has been studied for its potential as an anti-inflammatory, immunosuppressive agent, and inhibitor of cancer cell growth.
Antioxidant Properties
Exhibits antioxidant properties, which could potentially be valuable for protecting cells from oxidative damage.
Ongoing Research
Further research into the biological activities and potential medical applications of 2-(2-methyl-1H-indol-3-yl)-1,4-diphenylbutane-1,4-dione is ongoing.
Check Digit Verification of cas no
The CAS Registry Mumber 6339-47-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,3 and 9 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6339-47:
(6*6)+(5*3)+(4*3)+(3*9)+(2*4)+(1*7)=105
105 % 10 = 5
So 6339-47-5 is a valid CAS Registry Number.
6339-47-5Relevant academic research and scientific papers
Indirect regioselective heteroarylation of indoles through a Friedel-Crafts reaction with (E)-1,4-diaryl-2-buten-1,4-diones
Blay, Gonzalo,Fernández, Isabel,Monleón, Alicia,Pedro, José R.,Vila, Carlos
experimental part, p. 9264 - 9270 (2010/01/06)
A two-step synthesis of 3-heteroaryl indoles has been developed. The first step of the sequence involves a Friedel-Crafts alkylation of indoles with 1,4-diaryl-2-buten-1,4-diones to give the corresponding indoles bearing a 1,4-dicarbonyl moiety. The reaction is catalyzed by InCl3 and takes place with good yields. Cyclization of the diones under different Paal-Knorr conditions allows to prepare indoles substituted at the C3 position with 3-furanyl, 3-pyrrolyl- and 3-thienyl moieties.
