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2,3-diphenyl-5-(trifluoromethyl)quinoxaline is a quinoxaline derivative, a heterocyclic aromatic organic compound with the molecular formula C20H13F3N2. It is recognized for its diverse biological activities, such as potential antitumor, antiviral, and anti-inflammatory properties, and has been studied for its potential use as an anticancer agent and as a fluorescent probe.

389-61-7

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389-61-7 Usage

Uses

Used in Pharmaceutical Industry:
2,3-diphenyl-5-(trifluoromethyl)quinoxaline is used as a potential anticancer agent for its potential antitumor properties, which could be utilized in the development of new cancer treatments.
Used in Medical Research:
2,3-diphenyl-5-(trifluoromethyl)quinoxaline is used as a fluorescent probe, which can be employed in various research applications, such as cell imaging and the study of biological processes.
Used in Agrochemical Industry:
2,3-diphenyl-5-(trifluoromethyl)quinoxaline is used as a building block for the synthesis of various agrochemical compounds, leveraging its unique structural and chemical properties to develop new pesticides or other agricultural products.
Used in Chemical Synthesis:
2,3-diphenyl-5-(trifluoromethyl)quinoxaline is used as a key intermediate in the synthesis of pharmaceutical compounds, contributing to the development of new drugs with potential therapeutic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 389-61-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,8 and 9 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 389-61:
(5*3)+(4*8)+(3*9)+(2*6)+(1*1)=87
87 % 10 = 7
So 389-61-7 is a valid CAS Registry Number.

389-61-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-diphenyl-5-(trifluoromethyl)quinoxaline

1.2 Other means of identification

Product number -
Other names 2,3-diphenyl-5-trifluoromethyl-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:389-61-7 SDS

389-61-7Downstream Products

389-61-7Relevant academic research and scientific papers

One-pot synthesis of quinoxalines from reductive coupling of 2-nitroanilines and 1,2-diketones using indium

Go, Ahra,Lee, Geunsoo,Kim, Jaeho,Bae, Seolhee,Lee, Byung Min,Kim, Byeong Hyo

, p. 1215 - 1226 (2015/03/04)

The one-pot reduction-cyclization of 2-nitroanilines and 1,2-diketones to give quinoxalines was investigated. Using indium and an appropriate acid such as acetic acid or indium(III) chloride, various quinoxaline derivatives including 2,3-dialkylquinoxalines, 2,3-diphenylquinoxalines, 2,3-di-2-thiophenylquinoxalines, 2,3-di(pyridin-2-yl)quinoxalines, and dibenzo[a,c]phenazines were synthesized in moderate to excellent yield.

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