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107384-68-9

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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.

107384-68-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1H-Pyrrolo<3,2-c>pyridin-6-carbonsaeure-ethylester

1.2 Other means of identification

Product number -
Other names ethyl 1H-indole-6-carboxylate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:107384-68-9 SDS

107384-68-9Downstream Products

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.

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