1333429-65-4 Usage
Uses
Used in Pharmaceutical Industry:
(E)-3-(1,2-dimethyl-1H-indol-3-yl)acrylaldehyde is used as a building block in organic synthesis, particularly for the creation of various pharmaceutically active compounds. Its unique structure and properties make it a valuable starting material in the development of new drugs and therapeutic agents.
Used in Organic Synthesis:
In the field of organic synthesis, (E)-3-(1,2-dimethyl-1H-indol-3-yl)acrylaldehyde serves as a key intermediate for the synthesis of a wide range of chemical products. Its reactivity and structural features allow for the formation of diverse molecules with potential applications in various industries, including pharmaceuticals, agrochemicals, and materials science.
Check Digit Verification of cas no
The CAS Registry Mumber 1333429-65-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,3,4,2 and 9 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1333429-65:
(9*1)+(8*3)+(7*3)+(6*3)+(5*4)+(4*2)+(3*9)+(2*6)+(1*5)=144
144 % 10 = 4
So 1333429-65-4 is a valid CAS Registry Number.
1333429-65-4Relevant academic research and scientific papers
A novel entry to functionalized benzofurans and indoles via palladium(0)-catalyzed arylative dearomatization of furans
Yin, Biaolin,Cai, Congbi,Zeng, Guohui,Zhang, Ruoqi,Li, Xiang,Jiang, Huanfeng
, p. 1098 - 1101 (2012/03/27)
A novel entry to functionalized benzofurans and indoles from furans in moderate to good yields has been developed. This protocol involves palladium(0)-catalyzed dearomatizing intramolecular arylation of the furan ring, formation of a π-allylic palladium complex, furan ring opening, and a β-hydride elimination sequence.
Asymmetric catalysis of Diels-Alder reactions with in situ generated heterocyclic ortho -quinodimethanes
Liu, Yankai,Nappi, Manuel,Arceo, Elena,Vera, Silvia,Melchiorre, Paolo
, p. 15212 - 15218 (2011/11/13)
The Diels-Alder reaction is probably the most powerful technology in the synthetic repertoire for single-step constructions of complex chiral molecules. The synthetic power of this fundamental pericyclic transformation has greatly increased with the emerg
