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138476-26-3

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138476-26-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 138476-26-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,4,7 and 6 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 138476-26:
(8*1)+(7*3)+(6*8)+(5*4)+(4*7)+(3*6)+(2*2)+(1*6)=153
153 % 10 = 3
So 138476-26-3 is a valid CAS Registry Number.

138476-26-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-bis(4-chlorophenyl)quinoxaline

1.2 Other means of identification

Product number -
Other names Quinoxaline,2,3-bis(4-chlorophenyl)

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:138476-26-3 SDS

138476-26-3Downstream Products

138476-26-3Relevant articles and documents

An efficient and recyclable nanoparticle-supported cobalt catalyst for quinoxaline synthesis

Rajabi, Fatemeh,Alves, Diego,Luque, Rafael

, p. 20709 - 20718 (2015)

The syntheses of quinoxalines derived from 1,2-diamine and 1,2-dicarbonyl compounds under mild reaction conditions was carried out using a nanoparticle-supported cobalt catalyst. The supported nanocatalyst exhibited excellent activity and stability and it

NaOH-Mediated Direct Synthesis of Quinoxalines from o-Nitroanilines and Alcohols via a Hydrogen-Transfer Strategy

Wang, Yan-Bing,Shi, Linlin,Zhang, Xiaojie,Fu, Lian-Rong,Hu, Weinan,Zhang, Wenjing,Zhu, Xinju,Hao, Xin-Qi,Song, Mao-Ping

, p. 947 - 958 (2021/01/14)

A NaOH-mediated sustainable synthesis of functionalized quinoxalines is disclosed via redox condensation of o-nitroamines with diols and α-hydroxy ketones. Under optimized conditions, various o-nitroamines and alcohols are well tolerated to generate the desired products in 44-99% yields without transition metals and external redox additives.

Quinoxaline derivatives and application thereof in organic light-emitting devices

-

Paragraph 0038-0042, (2020/06/20)

The present invention discloses a novel organic compound having a structure represented by the formula shown in the specification, wherein L1 and L2 are each independently selected from one of a single bond, a substituted or unsubstituted C6-C30 arylene group, and a substituted or unsubstituted C3-C30 heteroarylene group, wherein Ar1 is selected from one of substituted or unsubstituted C3-C30 heteroaryl groups containing at least two heteroatoms, and Ar2 is selected from one of substituted or unsubstituted C6-C30 aryl groups and substituted or unsubstituted C3-C30 heteroaryl groups. When the compound provided by the invention is used as a luminescent material in an OLED device, excellent device performance and stability are shown. The invention also discloses an organic light-emitting device adopting the compound with the general formula.

Dowex 50W: Mild efficient reusable heterogeneous catalyst for synthesis of quinoxaline derivatives in aqueous medium

Datta, Arup,Halder, Samiran

, p. 1218 - 1224 (2021/02/09)

An efficient, simple and eco-friendly procedure is reported in presence of heterogeneous Dowex 50W catalyst in aqueous medium under refluxing condition to produce quinoxaline derivatives. Catalyst has participated in condensation reaction between 1,2-diamines and various aromatic 1,2-diketones smoothly with excellent yield of the products in short reaction times. Dowex 50W was used more than five times in this reaction separately and showed an excellent recyclability throughout the reaction.(figure presented).

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