66824-94-0 Usage
Uses
Used in Organic Synthesis:
Ethyl 2-[(2-chlorobenzoyl)amino]acetate is utilized as a key intermediate in the synthesis of various organic molecules, particularly in the preparation of pharmaceuticals and agrochemicals. Its unique structure allows for the creation of a wide range of compounds with diverse applications.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, ethyl 2-[(2-chlorobenzoyl)amino]acetate is used as a building block for the development of new drugs. Its incorporation into drug molecules can potentially enhance their therapeutic effects and properties, contributing to the advancement of medicinal chemistry.
Used in Agrochemical Industry:
Ethyl 2-[(2-chlorobenzoyl)amino]acetate also finds application in the agrochemical industry, where it serves as a precursor for the synthesis of various agrochemicals. Its use in this field can lead to the development of more effective and targeted pesticides and other agricultural products.
Used in Research and Development:
Due to its potential pharmacological properties, ethyl 2-[(2-chlorobenzoyl)amino]acetate is employed in research and development for studying its anti-inflammatory and analgesic effects. This can pave the way for the discovery of new therapeutic agents and treatments for various medical conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 66824-94-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,8,2 and 4 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 66824-94:
(7*6)+(6*6)+(5*8)+(4*2)+(3*4)+(2*9)+(1*4)=160
160 % 10 = 0
So 66824-94-0 is a valid CAS Registry Number.
InChI:InChI=1/C11H12ClNO3/c1-2-16-10(14)7-13-11(15)8-5-3-4-6-9(8)12/h3-6H,2,7H2,1H3,(H,13,15)
66824-94-0Relevant academic research and scientific papers
Substituents effect on the erlenmeyer-ploechl reaction: Understanding an observed process reaction time
Chavez, Flavio,Kennedy, Nicole,Rawalpally, Thimma,Williamson, R. Thomas,Cleary, Thomas
experimental part, p. 579 - 584 (2011/07/08)
A systematic study on hippuric acid substituents was performed in order to better understand the influence of stereoelectronic factors on the Erlenmeyer reaction rate. In addition, two reaction systems were evaluated: Huenig's base solvent free conditions and catalytic sodium acetate in 2-methyl-THF. The effect on reaction rate of electron withdrawing and electron donating groups are reported. Specifically, the study led to the conclusion that stereoelectronic factors have significant influence in one of our key Erlenmeyer reaction by affecting its reaction rate.
An efficient one-pot synthesis of hippuric acid ethyl ester derivatives
Conway, Samuel C.,Perni, Robert B.
, p. 1539 - 1545 (2007/10/03)
A rapid, one-pot procedure is described for the preparation of the ethyl esters of a number of ring-substituted N-benzoyl glycine (hippuric acid) derivatives from readily-available starling materials.
