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1195622-96-8

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1195622-96-8 Usage

Derivative of pyrrolopyridine

This compound belongs to the pyrrolopyridine class, which has potential biological and pharmacological activities.

Common use in synthesis

The chemical is frequently used in the synthesis of pharmaceuticals and agrochemicals, indicating its importance in creating various drugs and chemicals used in agriculture.

Intermediate in production

It serves as an intermediate in the production of different organic compounds, making it a crucial component in multiple chemical reactions.

Ethyl ester group

The presence of the ethyl ester group in the molecule imparts specific chemical properties to the compound, making it suitable for a variety of chemical processes and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1195622-96-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,5,6,2 and 2 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1195622-96:
(9*1)+(8*1)+(7*9)+(6*5)+(5*6)+(4*2)+(3*2)+(2*9)+(1*6)=178
178 % 10 = 8
So 1195622-96-8 is a valid CAS Registry Number.

1195622-96-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl 1H-pyrrolo[2,3-b]pyridine-3-carboxylate

1.2 Other means of identification

Product number -
Other names -

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:1195622-96-8 SDS

1195622-96-8Relevant articles and documents

Acrosin structure-based design, synthesis and biological activities of 7-azaindol derivatives as new acrosin inhibitors

Jiang, Jun Hang,Liu, Xue Fei,Zhen, Can Hui,Zhou, You Jun,Zhu, Ju,Lv, Jia Guo,Sheng, Chun Quan

scheme or table, p. 272 - 275 (2012/01/14)

A series of 7-azaindol derivatives were designed based on the homologous 3D model of human acrosin. These compounds were synthesized and evaluated for their human acrosin inhibitory activities in vitro. Compounds 7a, 7i, 7j, 7k and 7n showed highly inhibitory activity against human acrosin. The three-dimensional structure-activity relationship was investigated through a CoMFA model, which provided valuable information to further study of potential human acrosin inhibitors.

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