19747-79-6 Usage
Uses
Used in Pharmaceutical Industry:
1H-Indole-3-carboximidic acid ethyl ester is used as an intermediate in the synthesis of various pharmaceuticals for its potential antifungal and anti-inflammatory properties. Its enhanced solubility and bioavailability make it a valuable component in the development of new drugs and therapeutic agents.
Used in Agrochemical Industry:
1H-Indole-3-carboximidic acid ethyl ester is used as a precursor in the synthesis of various agrochemicals, contributing to the development of effective and efficient products for agricultural applications.
Used in Drug Development:
1H-Indole-3-carboximidic acid ethyl ester is used as a potential candidate in the development of new drugs and therapeutic agents, given its reported biological activities and its role as a valuable intermediate in pharmaceutical synthesis.
Check Digit Verification of cas no
The CAS Registry Mumber 19747-79-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,7,4 and 7 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 19747-79:
(7*1)+(6*9)+(5*7)+(4*4)+(3*7)+(2*7)+(1*9)=156
156 % 10 = 6
So 19747-79-6 is a valid CAS Registry Number.
19747-79-6Relevant academic research and scientific papers
SYNTHESIS AND PROPERTIES OF AZOLES AND THEIR DERIVATIVES. 32. SYNTHESIS AND SOME TRANSFORMATIONS OF HYDROCHLORIDES OF IMIDO ESTERS OF INDOLECARBOXYLIC ACIDS
Kelarev, V. I.,Shvekhgeimer, G. A.
, p. 501 - 506 (2007/10/02)
The Pinner reaction with the nitriles of indole-3-carboxylic and 3-indolylacetic acids was studied.The hydrochlorides of the imide esters of these acids, which were converted to the free bases, amides, and esters, were synthesized.Imidazolines, benzimidazoles, and benzoxazoles that contain indole substituents were obtained by condensation of the hydrochlorides of the imido esters of the indolecarboxylic acids with ethylenediamine, o-phenylenediamine, and o-aminophenol.
