107384-68-9 Usage
General Description
1H-Pyrrolo[3,2-c]pyridine-6-carboxylic acid, ethyl ester, also known as ethyl 1H-pyrrolo[3,2-c]pyridine-6-carboxylate, is a chemical compound commonly used in the pharmaceutical industry. It is derived from the pyrrolopyridine class of compounds and is often utilized as a building block in the synthesis of various pharmaceutical drugs. 1H-Pyrrolo[3,2-c]pyridine-6-carboxylic acid, ethyl ester has been found to exhibit a range of biological activities, including anti-inflammatory and anticancer properties, and is being studied for its potential therapeutic applications. It is typically produced through esterification of 1H-pyrrolo[3,2-c]pyridine-6-carboxylic acid with ethanol, and its chemical structure makes it a versatile intermediate for the development of novel drug candidates.
Check Digit Verification of cas no
The CAS Registry Mumber 107384-68-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,3,8 and 4 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 107384-68:
(8*1)+(7*0)+(6*7)+(5*3)+(4*8)+(3*4)+(2*6)+(1*8)=129
129 % 10 = 9
So 107384-68-9 is a valid CAS Registry Number.
107384-68-9Relevant articles and documents
Reactions with 2-Aza-1,3-butadiene Derivatives, 2.- A Facile Access to the Pyrrolopyrimidine and Pyrrolopyridine System
Biere, Helmut,Russe, Rolf
, p. 491 - 494 (2007/10/02)
3-Methylindole (4) as well as pyrrole derivatives 7 react under proton catalysis with 2-azabutadiene 2a in the α-position.The subsequent ring closure into a free neighbouring position (N or C), which is also affected by further substituents, furnishes the pyrrolopyrimidine 5 and 8, resp., and/or the pyrrolopyridine 9.