205873-58-1 Usage
Description
Indole-7-carboxylic acid ethyl ester is a versatile chemical compound belonging to the indole class of organic compounds. It is characterized by its distinct odor and is widely used in various industries, including pharmaceuticals, agrochemicals, perfumery, and the food industry. Its potential biological activities, such as anti-inflammatory and anticancer effects, further expand its range of applications.
Uses
Used in Pharmaceutical and Agrochemical Industries:
Indole-7-carboxylic acid ethyl ester is used as a key intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its unique chemical structure allows for the development of new drugs and pesticides with improved efficacy and safety profiles.
Used in Perfumery and Fragrance Industry:
Indole-7-carboxylic acid ethyl ester is used as a fragrance ingredient in the perfumery and fragrance industry. Its distinct odor makes it a valuable component in creating complex and appealing scents for a wide range of products, including perfumes, colognes, and scented cosmetics.
Used in Food Industry:
Indole-7-carboxylic acid ethyl ester is used as a flavoring agent in the food industry. Its unique taste and aroma enhance the sensory experience of various food products, contributing to their overall appeal and consumer satisfaction.
Used in Research and Development:
Indole-7-carboxylic acid ethyl ester is used in research and development for exploring its potential biological activities. Studies have shown that it possesses anti-inflammatory and anticancer properties, making it a promising candidate for the development of new therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 205873-58-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,5,8,7 and 3 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 205873-58:
(8*2)+(7*0)+(6*5)+(5*8)+(4*7)+(3*3)+(2*5)+(1*8)=141
141 % 10 = 1
So 205873-58-1 is a valid CAS Registry Number.
InChI:InChI=1/C11H11NO2/c1-2-14-11(13)9-5-3-4-8-6-7-12-10(8)9/h3-7,12H,2H2,1H3
205873-58-1Relevant articles and documents
RhCl3·3H2O-Catalyzed C7-Selective C-H Carbonylation of Indolines with CO and Alcohols
Du, Rongrong,Zhao, Kang,Liu, Jianhua,Han, Feng,Xia, Chungu,Yang, Lei
, p. 6418 - 6422 (2019)
An attractive method for the synthesis of indoline-7-carboxylates through RhCl3-catalyzed C-H carbonylation of indolines with CO and alcohols was developed. The copper-based oxidant and removable pyrimidyl directing group played important roles in achieving high-level yields of the title products. Based on control experiments, a possible catalytic cycle was proposed.
Noncovalent Interactions in Ir-Catalyzed C-H Activation: L-Shaped Ligand for Para-Selective Borylation of Aromatic Esters
Hoque, Md Emdadul,Bisht, Ranjana,Haldar, Chabush,Chattopadhyay, Buddhadeb
supporting information, p. 7745 - 7748 (2017/06/21)
An efficient strategy for the para-selective borylation of aromatic esters is described. For achieving high para-selectivity, a new catalytic system has been developed modifying the core structure of the bipyridine. It has been proposed that the L-shaped ligand is essential to recognize the functionality of the oxygen atom of the ester carbonyl group via noncovalent interaction, which provides an unprecedented controlling factor for para-selective C-H activation/borylation.
A new one-pot synthesis of polysubstituted indoles from pyrroles and β-nitroacrylates
Palmieri, Alessandro,Gabrielli, Serena,Lanari, Daniela,Vaccaro, Luigi,Ballini, Roberto
experimental part, p. 1425 - 1428 (2011/08/03)
The reaction of β-nitroacrylates with pyrroles, under solvent- and catalyst-free conditions, allows the formation of Friedel-Crafts adducts which, after in situ treatment with Amberlyst 15 in isopropyl alcohol under reflux, provide polysubstituted indoles, via a benzannulation reaction, in a one-pot process. Copyright