93957-50-7 Usage
Description
(E)-3-[3'-(4"-Fluorophenyl)-1'-(1"-methylethyl)-1H-indol-2"-yl]-2-propnal is a synthetic organic compound characterized by a complex molecular structure that features an indole ring, a propenal group, and a fluorophenyl group. As a derivative of indole, this compound is heterocyclic and aromatic, with potential applications in medicinal chemistry due to its structural similarity to other bioactive compounds. The incorporation of fluorophenyl and propenal groups also indicates its possible utility in organic synthesis and materials science, although further research and testing are required to elucidate its full properties and potential uses.
Uses
Used in Medicinal Chemistry:
(E)-3-[3'-(4"-Fluorophenyl)-1'-(1"-methylethyl)-1H-indol-2"-yl]-2-propnal is used as a potential bioactive molecule for the development of new pharmaceutical agents, leveraging its structural resemblance to other compounds with known biological activity. Its unique combination of functional groups may contribute to novel mechanisms of action or enhanced pharmacological properties.
Used in Organic Synthesis:
In the field of organic synthesis, (E)-3-[3'-(4"-Fluorophenyl)-1'-(1"-methylethyl)-1H-indol-2"-yl]-2-propnal serves as a building block or intermediate in the synthesis of more complex organic molecules. Its fluorophenyl and propenal groups can be strategically modified to create a variety of new compounds with tailored properties.
Used in Materials Science:
(E)-3-[3'-(4"-Fluorophenyl)-1'-(1"-methylethyl)-1H-indol-2"-yl]-2-propnal is utilized in materials science for the development of new materials with specific properties. (E)-3-[3'-(4"-Fluorophenyl)-1'-(1"-methylethyl)-1H-indol-2"-yl]-2-propnal's molecular structure may contribute to the creation of materials with unique electronic, optical, or mechanical characteristics, depending on its interaction with other molecules or its self-assembly behavior.
Check Digit Verification of cas no
The CAS Registry Mumber 93957-50-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,9,5 and 7 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 93957-50:
(7*9)+(6*3)+(5*9)+(4*5)+(3*7)+(2*5)+(1*0)=177
177 % 10 = 7
So 93957-50-7 is a valid CAS Registry Number.
93957-50-7Relevant articles and documents
Br?nsted Acids Enable Three Molecular Rearrangements of One 3-Alkylidene-2H-1,2-oxazine Molecule into Distinct Heterocyles
Mokar, Bhanudas Dattatray,Liu, Jinxian,Liu, Rai-Shung
, p. 1038 - 1041 (2018/02/23)
This work describes three different strategies to structurally rearrange one 3-alkylidene-2H-1,2-oxazine molecule into three distinct heterocycles using HOTf, propiolic acid, and silica gel, respectively. The mechanisms of these rearrangement reactions in
Palladium-catalyzed synthesis of 2-alkenyl-3-arylindoles via a dual α-arylation strategy: Formal synthesis of the antilipemic drug fluvastatin
Kale, Ajit Prabhakar,Kumar, Gangam Srikanth,Kapur, Manmohan
, p. 10995 - 11002 (2015/11/25)
A new approach has been developed for the synthesis of substituted 2-alkenyl-3-arylindoles. The strategy comprises palladium-catalyzed dual α-arylation of TES-enol ethers of enones as the key step. This methodology results in products with very good yields and the regioselectivity is exclusive. We have also successfully used this dual α-arylation methodology in the formal synthesis of the cholesterol-lowering drug fluvastatin.
Process for the synthesis of N-methyl-N-phenylaminoacrolein
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Page column 5 - 6, (2008/06/13)
A process is disclosed for manufacturing N-methyl-N-phenylaminoacrolein of formula (I) which comprises reacting N-methylformanilide and an alkyl vinyl ether of formula (III) wherein R is a C3-C4 alkyl, said process being characterize
Xi:Irritant;
