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69737-10-6

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69737-10-6 Usage

General Description

1-(2-chlorophenyl)-2-(quinoxalin-2-yl)ethenamine, also known as CX-157, is a novel chemical compound with potential pharmacological properties. It belongs to the class of phenyl ethenamines and contains a chlorophenyl and quinoxalin-2-yl group. CX-157 has shown to exhibit psychoactive and cognitive-enhancing effects in animal studies, and it is of interest for its potential use in treating cognitive disorders such as Alzheimer's disease. It is a promising compound for further research and development in the field of neuroscience and drug discovery.

Check Digit Verification of cas no

The CAS Registry Mumber 69737-10-6 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 0 respectively.
Calculate Digit Verification of CAS Registry Number 69737-10:
(7*6)+(6*9)+(5*7)+(4*3)+(3*7)+(2*1)+(1*0)=166
166 % 10 = 6
So 69737-10-6 is a valid CAS Registry Number.

69737-10-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-chlorophenyl)-2-quinoxalin-2-ylethenamine

1.2 Other means of identification

Product number -
Other names 1-(2-chlorophenyl)-2-propanone

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:69737-10-6 SDS

69737-10-6Downstream Products

69737-10-6Relevant 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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