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119580-84-6

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119580-84-6 Usage

Structure

A five-membered aromatic ring containing four carbon atoms and one nitrogen atom, with a carbonitrile functional group and an ethenyl and methyl substituent.

Reactivity

Highly reactive

Toxicity

Potentially toxic

Uses

Commonly used in organic synthesis and pharmaceutical research due to its ability to participate in a variety of chemical reactions. Has potential applications in the development of new drugs and materials.

Handling precautions

Caution should be exercised when handling this compound due to its potential hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 119580-84-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,5,8 and 0 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 119580-84:
(8*1)+(7*1)+(6*9)+(5*5)+(4*8)+(3*0)+(2*8)+(1*4)=146
146 % 10 = 6
So 119580-84-6 is a valid CAS Registry Number.

119580-84-6SDS

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 1H-Pyrrole-2-carbonitrile,4-ethenyl-1-methyl-(9CI)

1.2 Other means of identification

Product number -
Other names 2-Quinazolinecarbonitrile,1,4-dihydro-1-methyl-4-oxo

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:119580-84-6 SDS

119580-84-6Downstream Products

119580-84-6Relevant articles and documents

PYRROLE STUDIES. PART 40. SYNTHESIS OF 2- AND 3-SUBSTITUTED 1-METHYLINDOLES FROM VINYLPYRROLES.

Gonsalez-Rosende, Eugenia,Jones, R. Alan,Sepulveda-Arques, Jose,Zaballos-Garcia, Elena

, p. 1669 - 1678 (2007/10/02)

4-Substituted-2-vinylpyrroles are more reactive than 2-substituted-4-vinylpyrroles in their reaction with DMAD to yield, respectively, 6,7- and 4,5-dihydroindoles, which are readily dehydrogenated to give indoles possessing electron-withdrawing substituents at the 3- and 2-positions.

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