57642-05-4 Usage
Description
1-(1H-Indol-3-Yl)-2-Iodo-Ethanone, also known as 3-indole-2-iodopropan-1-one, is a chemical compound characterized by the molecular formula C10H8INO. It is a derivative of indole, featuring a ketone and an iodo group within its structure. 1-(1H-Indol-3-Yl)-2-Iodo-Ethanone is recognized for its potential biological activity and is frequently utilized in the realms of organic synthesis and pharmaceutical research.
Uses
Used in Pharmaceutical Research:
1-(1H-Indol-3-Yl)-2-Iodo-Ethanone is used as a research compound for its potential anti-cancer properties. It is investigated for its ability to target and inhibit specific cancer cell pathways, thereby exhibiting promise as a therapeutic agent in oncology.
Used in Organic Synthesis:
In the field of organic chemistry, 1-(1H-Indol-3-Yl)-2-Iodo-Ethanone serves as a valuable precursor for the synthesis of other pharmaceutical compounds. Its unique structure allows for the creation of a variety of molecules with potential applications in medicine and other industries.
Used in Chemical Compound Development:
1-(1H-Indol-3-Yl)-2-Iodo-Ethanone is also utilized as a starting material in the development of new chemical compounds. Its versatility and reactivity make it a popular choice for researchers looking to create novel substances with specific properties and potential uses.
Check Digit Verification of cas no
The CAS Registry Mumber 57642-05-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,6,4 and 2 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 57642-05:
(7*5)+(6*7)+(5*6)+(4*4)+(3*2)+(2*0)+(1*5)=134
134 % 10 = 4
So 57642-05-4 is a valid CAS Registry Number.
57642-05-4Relevant articles and documents
Mild and General Synthesis of Pyrrolo[2,1-a]isoquinolines and Related Polyheterocyclic Frameworks from Pyrrole Precursors Derived from a Mechanochemical Multicomponent Reaction
Leonardi, Marco,Villacampa, Mercedes,Menéndez, J. Carlos
, p. 2570 - 2578 (2017/03/14)
The combination of a three-component, solvent-free pyrrole synthesis performed under mechanochemical conditions with a TMSOTf-catalyzed oxonium-mediated cyclization gave general access to pyrrolo[2,1-a]isoquinoline derivatives under very mild conditions.
Logic design and synthesis of quinoxalines via the integration of iodination/oxidation/cyclization sequences from ketones and 1,2-diamines
Lian, Mi,Li, Qi,Zhu, Yanping,Yin, Guodong,Wu, Anxin
, p. 9598 - 9605 (2012/11/07)
A novel protocol for the synthesis of quinoxalines has been developed from simple ketones and 1,2-diamines. This process underwent a logic approach to bis-substituted quinoxalines via a consecutive iodination/Kornblum oxidation/cyclization in the presence of I2/CuO/DMSO and to mono-substituted quinoxalines via an iodination/cyclization/aromatization in the presence of I2/CuO/K3PO4·3H 2O.