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N-(4-bromophenyl)-N-(2-[(4-bromophenyl)imino]-1(2H)-acenaphthylenylidene)amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

266340-77-6

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266340-77-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 266340-77-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,6,3,4 and 0 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 266340-77:
(8*2)+(7*6)+(6*6)+(5*3)+(4*4)+(3*0)+(2*7)+(1*7)=146
146 % 10 = 6
So 266340-77-6 is a valid CAS Registry Number.

266340-77-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-N,2-N-bis(4-bromophenyl)acenaphthylene-1,2-diimine

1.2 Other means of identification

Product number -
Other names Benzenamine,N,N'-1,2-acenaphthylenediylidenebis[4-bromo

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:266340-77-6 SDS

266340-77-6Downstream Products

266340-77-6Relevant academic research and scientific papers

Potent half-sandwich Ru(Ⅱ) N^N (aryl-BIAN) complexes: Lysosome-mediated apoptosis, in vitro and in vivo anticancer activities

Xu, Zhishan,Huang, Jie,Kong, Deliang,Yang, Yuliang,Guo, Lihua,Jia, Xianglei,Zhong, Genshen,Liu, Zhe

, (2020/09/02)

Herein a new series of organometallic half-sandwich Ru(Ⅱ) complexes bearing aryl-BIAN chelating ligands with various electron-withdrawing and electron-donating substituents have been developed as theranostic agents. All the complexes display much higher anti-proliferative potency than the clinical chemotherapeutic drug cisplatin towards seven cancer cell lines. The anti-proliferative efficacy of these complexes is correlated to their electron-withdrawing ability. Interestingly, complex Ru1 also potently suppresses cancer cell migration in vitro and effectively inhibit tumor growth in vivo in a CT26 colon cancer mouse xenograft model. Mechanisms of action studies display that Ru1 can favorably accumulate in lysosome and exerts anti-cancer potency by inducing a series of events related to lysosomal dysfunction in CT26 cells. Interestingly, inhibition of lysosomal enzymes leads to suppression of cytotoxicity and apoptosis induced by Ru1. Our results elucidate that complex Ru1 can elicit cytotoxicity through lysosome-mediated apoptosis in vitro and suppress tumor growth in vivo.

A multi-step solvent-free mechanochemical route to indium(III) complexes

Wang, Jingyi,Ganguly, Rakesh,Yongxin, Li,Díaz, Jesus,Soo, Han Sen,García, Felipe

supporting information, p. 7941 - 7946 (2016/06/01)

Mechanochemistry is well-established in the solid-phase synthesis of inorganic materials but has rarely been employed for molecular syntheses. In recent years, there has been nascent interest in 'greener' synthetic methods with less solvent, higher yields, and shorter reaction times being especially appealing to the fine chemicals and inorganic catalyst industries. Herein, we demonstrate that main-group indium(iii) complexes featuring bis(imino)acenaphthene (BIAN) ligands are readily accessible through a mechanochemical milling approach. The synthetic methodology reported herein not only bypasses the use of large solvent quantities and transition metal reagents for ligand synthesis, but also reduces reaction times dramatically. These new main-group complexes exhibit the potential to be reduced to indium(i) compounds, which may be employed as photosensitizers in organic catalyses and functional materials.

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