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69737-11-7

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69737-11-7 Usage

General Description

1-(2-chlorophenyl)-2-(3-phenylquinoxalin-2-yl)ethenamine is a chemical compound that is a derivative of quinoxaline and ethenamine. It consists of a chlorophenyl group attached to a quinoxaline-2-yl group, which in turn is attached to an ethenamine group. 1-(2-chlorophenyl)-2-(3-phenylquinoxalin-2-yl)ethenamine has potential biological activity and may be used in pharmaceutical research for its potential therapeutic effects. The specific properties, uses, and potential hazards of this compound would need to be determined through further research and testing.

Check Digit Verification of cas no

The CAS Registry Mumber 69737-11-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,7,3 and 7 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 69737-11:
(7*6)+(6*9)+(5*7)+(4*3)+(3*7)+(2*1)+(1*1)=167
167 % 10 = 7
So 69737-11-7 is a valid CAS Registry Number.

69737-11-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (Z)-1-(2-chlorophenyl)-2-(3-phenylquinoxalin-2-yl)ethenamine

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:69737-11-7 SDS

69737-11-7Downstream Products

69737-11-7Relevant articles and documents

Action d'organolithiens sur la methyl-2 quinoxaline. Etude de la reactivite des adduits

Mettey, Yvette,Vierfond, Jean-Michel,Thal, Claude,Miocque, Marcel

, p. 133 - 137 (2007/10/02)

The action of organolithium reagents such as phenyllithium or n-butyllithium on 2-methylquinoxaline gave lithiation of the methyl group which upon reaction with electrophiles produce side chain alkenyl derivatives.On the other hand organolithium reagents react with the quinoxaline azomethine bond to give 1-lithio-2-alkyl(or aryl)-3-methylquinoxalines which can be further lithiated on the methyl group to give 2-alkyl(or aryl)-3-alkenylquinoxaline derivatives.The adducts can be condensed with electrophiles such as benzonitrile or methyl benzoate but only methyl benzoate leads to N condensed derivatives.Furthermore substituted 1,2,3,4-tetraquinoxalines are available via the above lithio intermediates.

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