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86268-06-6

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86268-06-6 Usage

General Description

(3-methyl-2,3-diphenyl-3,4-dihydroquinoxalin-1(2H)-yl)(phenyl)methanone, also known as BAY 13-9952, is a chemical compound with potential pharmaceutical applications. It is a quinoxaline derivative that has been studied for its potential in treating a variety of medical conditions, including cancer and neurological disorders. Quinoxaline derivatives are known for their diverse biological activities, including antibacterial, antiviral, antifungal, antitumor, and anti-inflammatory properties. BAY 13-9952 has been specifically investigated for its potential as a tyrosine kinase inhibitor, which could make it useful in the treatment of certain types of cancer. Its specific mechanisms of action and potential therapeutic uses continue to be explored through preclinical and clinical research.

Check Digit Verification of cas no

The CAS Registry Mumber 86268-06-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,2,6 and 8 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 86268-06:
(7*8)+(6*6)+(5*2)+(4*6)+(3*8)+(2*0)+(1*6)=156
156 % 10 = 6
So 86268-06-6 is a valid CAS Registry Number.

86268-06-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (3-methyl-2,3-diphenyl-2,4-dihydroquinoxalin-1-yl)-phenylmethanone

1.2 Other means of identification

Product number -
Other names Tetrahydro-1,2,3,4 methyl-3 diphenyl-2,3 benzoyl-1 quinoxaline

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:86268-06-6 SDS

86268-06-6Downstream Products

86268-06-6Relevant 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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