21422-40-2 Usage
Description
Methyl 2-(1H-indol-2-yl)acetate is a chemical compound with the molecular formula C12H13NO2. It is an indole derivative, which is a common structural motif found in many natural products and pharmaceuticals. methyl 2-(1H-indol-2-yl)acetate is known for its potential applications in various fields due to its unique chemical properties.
Uses
Used in Organic Synthesis:
Methyl 2-(1H-indol-2-yl)acetate is used as a building block in organic synthesis for the preparation of various indole-based compounds. Its versatile structure allows for the creation of a wide range of chemical entities, making it a valuable component in the development of new molecules.
Used in Pharmaceutical Industry:
As a starting material, methyl 2-(1H-indol-2-yl)acetate is utilized in the synthesis of pharmaceuticals. Its presence in the molecular structure of numerous bioactive compounds makes it an essential precursor in the development of new drugs with potential therapeutic applications.
Used in Agrochemicals:
Methyl 2-(1H-indol-2-yl)acetate also serves as a starting material in the synthesis of agrochemicals. Its role in creating compounds with pesticidal or herbicidal properties contributes to the advancement of agricultural solutions to enhance crop protection and yield.
Used in Medicinal Chemistry Research:
Due to its biological activities, methyl 2-(1H-indol-2-yl)acetate is an important target in medicinal chemistry research. Scientists explore its potential to contribute to the discovery of new therapeutic agents, particularly those that interact with biological systems in meaningful ways.
Check Digit Verification of cas no
The CAS Registry Mumber 21422-40-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,4,2 and 2 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 21422-40:
(7*2)+(6*1)+(5*4)+(4*2)+(3*2)+(2*4)+(1*0)=62
62 % 10 = 2
So 21422-40-2 is a valid CAS Registry Number.
21422-40-2Relevant articles and documents
Nucleophilic Additions to Pyridium Salts. Reduction of the Intermediate Dihydropyridines
Lavilla, Rodolfo,Gotsens, Teresa,Gullon, Francisco,Bosch, Joan
, p. 5233 - 5244 (1994)
Reduction of indolyldihydropyridines 4 and 5 satisfactorily gave the corresponding tetrahydropyridines 6 and 7.A similar reduction of 4-(2-indolylmethyl)-1,4-dihydropyridines 3 was inefficient.In contrast, dihydropyridine 19 was reduced to 23 and then cyclized to pentacycle 24.Direct cyclization of 19 resulted in the formation of imide 21.
Homolytic substitution reactions of electron-rich pentatomic heteroaromatics by electrophilic carbon-centered radicals. Synthesis of α-heteroarylacetic acids
Baciocchi,Muraglia,Sleiter
, p. 6817 - 6820 (2007/10/02)
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SYNTHESIS OF ELLIPTICINE
Weller, Dwight D.,Ford, Douglas W.
, p. 2105 - 2108 (2007/10/02)
The 6H-pyridocarbazole system is efficiently synthesized by intramolecular attack of an ester enolate on an unactivated pyridinium salt.
