56559-60-5 Usage
Uses
Used in Pharmaceutical Industry:
Indole-3-carboxylic acid, 1-methyl-, ethyl ester is used as an intermediate in the synthesis of various pharmaceuticals for its potential to contribute to the development of new drugs. Its role in organic synthesis allows for the creation of a wide range of medicinal compounds.
Used in Agrochemical Industry:
In the agrochemical sector, Indole-3-carboxylic acid, 1-methyl-, ethyl ester is used as a building block for the production of agrochemicals, potentially contributing to the development of new pesticides or other agricultural chemicals that can improve crop yields and protect plants from diseases and pests.
Used in Organic Synthesis:
Indole-3-carboxylic acid, 1-methyl-, ethyl ester is used as a key component in organic synthesis, enabling the creation of a variety of chemical compounds that can be applied across different industries, including the production of fine chemicals for various applications.
Used in Research and Development:
As a subject of research, Indole-3-carboxylic acid, 1-methyl-, ethyl ester is used in the exploration of its potential biological activity and applications in medicine and pharmacology. Its role in the synthesis of bioactive molecules makes it valuable for scientific studies aimed at discovering new therapeutic agents or understanding biological processes.
Check Digit Verification of cas no
The CAS Registry Mumber 56559-60-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,5,5 and 9 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 56559-60:
(7*5)+(6*6)+(5*5)+(4*5)+(3*9)+(2*6)+(1*0)=155
155 % 10 = 5
So 56559-60-5 is a valid CAS Registry Number.
56559-60-5Relevant academic research and scientific papers
Pd-catalyzed cascade reactions between: O -iodo- N -alkenylanilines and tosylhydrazones: Novel approaches to the synthesis of polysubstituted indoles and 1,4-dihydroquinolines
Paraja, Miguel,Valdés, Carlos
supporting information, p. 6312 - 6315 (2016/05/19)
Two different Pd-catalyzed cascade reactions between o-iodo-N-alkenylanilines and tosylhydrazones are described. The outcome of the cascade processes is determined by the substitution on the N-alkenyl fragment. The reactions with N-tosyl-N-ethylene-o-iodoanilines lead to indoles through a sequence that involves the sequential migratory insertions of a carbene ligand and a C-C double bond, featuring a 5-exo-trig cyclization. The reactions with N-alkyl-N-alkenyl-o-iodoanilines provide 1,4-dihydroquinolines through a cascade reaction that includes a formal 6-endo-trig cyclization. In both cases the benzofused heterocycles are built through the formation of two C-C bonds on the hydrazonic carbon atom.
