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122453-02-5

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122453-02-5 Usage

Structure

A pyrrole derivative with a carbonitrile group and a 4-chlorophenyl substituent

Usage

Commonly used in the pharmaceutical industry as a building block for the synthesis of various pharmaceutical drugs and active ingredients

Biological activities

Studied for its potential antifungal and anticancer properties

Versatility

Utilized in the development and production of various medicinal and pharmaceutical products.

Check Digit Verification of cas no

The CAS Registry Mumber 122453-02-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,4,5 and 3 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 122453-02:
(8*1)+(7*2)+(6*2)+(5*4)+(4*5)+(3*3)+(2*0)+(1*2)=85
85 % 10 = 5
So 122453-02-5 is a valid CAS Registry Number.

122453-02-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-Chlorophenyl)-1H-pyrrole-3-carbonitrile

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:122453-02-5 SDS

122453-02-5Relevant articles and documents

Application of 2-aryl substituted pyrrole compound in medicine for killing oncomelania hupensis

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Paragraph 0081; 0082; 0083; 0084, (2019/01/08)

The invention relates to an application of 2-aryl substituted pyrrole compound in a medicine for killing oncomelania hupensis and belongs to the technical field of prevention and treatment of bilharziasis, and particularly provides the chemical structure of the 2-aryl substituted pyrrole compound and a preparation method of same. The 2-aryl substituted pyrrole compound, being an active component,is used for preparing the snail killing agent in the forms of suspending agents, emulsions and micro-emulsions for killing the oncomelania hupensis. Immersion killing use amount of the 2-aryl substituted pyrrole compound being the active component of the snail killing agent is 0.1-10.00 mg/l, and immersion killing time is 24-72 h. The use amount of spray application is 1-10 g/m and action timeis 3-7 days. Experiment proves that the 2-aryl substituted pyrrole compound has killing activity on the oncomelania hupensis and is lower than a snail killing agent, niclosamide, in the prior art in toxicity on aquatic organisms. The compound can be processed to prepare the snail killing agents and applied in the field of prevention and treatment of bilharziasis.

Method of controlling phytopathogenic fungi

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, (2008/06/13)

This invention is directed to a method for the control of phytopathogenic fungi by contacting the same with a cyano- or nitroarylpyrrole compound, or by applying said pyrrole compound to the foliage of a plant susceptible to disease caused by said pathogens.

α-(2,3-Di(C1 -C4 alkoxy)ethylamino)-β-cyanostyrene and β-nitrostyrene compounds useful as intermediates in the preparation of insecticidal, acaricidal and nematicidal arylpyrroles and method for the preparation thereof

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, (2008/06/13)

This invention provides novel α-[2,2-di(C1 -C4 alkoxy)ethylamino]-β-cyanostyrene and α-[2,2-di(C1 -C4 alkoxy)ethylamino]-β-nitrostyrene compounds that are useful for the preparation of pesticidal arylpyrroles. T

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