19747-79-6 Usage
General Description
1H-Indole-3-carboximidic acid ethyl ester is a chemical compound with the molecular formula C11H12N2O2. It is a derivative of indole, a heterocyclic aromatic organic compound, and is commonly used in the synthesis of various pharmaceuticals and agrochemicals. 1H-INDOLE-3-CARBOXIMIDIC ACID ETHYL ESTER has been reported to exhibit diverse biological activities, including antifungal and anti-inflammatory properties. Its ethyl ester form likely enhances its solubility and bioavailability, making it a valuable intermediate in the production of pharmaceuticals and other organic compounds. Additionally, 1H-Indole-3-carboximidic acid ethyl ester may have potential applications in the development of new drugs and therapeutic agents. Overall, this chemical compound has significant importance in both the pharmaceutical and chemical industries for its various potential uses.
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 articles and documents
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.
