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255829-24-4

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255829-24-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 255829-24-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,5,8,2 and 9 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 255829-24:
(8*2)+(7*5)+(6*5)+(5*8)+(4*2)+(3*9)+(2*2)+(1*4)=164
164 % 10 = 4
So 255829-24-4 is a valid CAS Registry Number.

255829-24-4SDS

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 3,6-dibromo-9-(4-nitrophenyl)carbazole

1.2 Other means of identification

Product number -
Other names 9H-Carbazole,3,6-dibromo-9-(4-nitrophenyl)

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:255829-24-4 SDS

255829-24-4Relevant articles and documents

Effects on the electrochemical and electrochromic properties of 3,6 linked polycarbazole derivative by the introduction of different acceptor groups and copolymerization

Hu, Bin,Lv, Xiaojing,Sun, Jingwei,Bian, Gaofeng,Ouyang, Mi,Fu, Zhiyan,Wang, Pingjing,Zhang, Cheng

, p. 1521 - 1530 (2013)

Two novel donor-acceptor type monomers, ethyl 4-(3,6-di(thiophen-2-yl)-9H- carbazole-9-yl)-benzoate (ETCB) and 9-(4-nitrophenyl)-3,6-di(thiophen-2-yl)-9H- carbazole (NDTC), were synthesized and characterized. Both the monomers show good electrochemical ac

Synthesis of nitrocarbazole compounds and their electrocatalytic oxidation of alcohol

Zhu, Yinghong,Zhang, Jianqing,Chen, Ziying,Zhang, Anlun,Ma, Chunan

, p. 533 - 538 (2016/04/20)

Three compounds with nitrocarbazole frameworks were synthesized and their electrochemical reversibility as organic electrocatalysts was studied by cyclic voltammetry. The electrochemical reversibility and oxidation-reduction potential of the compounds were greatly affected by their substituents. The oxidation-reduction potential of the compound with an electron-donating group was negative, while that of the compound with an electron-withdrawing group on the carbazole framework was positive. The electrocatalytic oxidation activities of the nitrocarbazole compounds were investigated through cyclic voltammetry and controlled potential electrolysis at room temperature. The electrocatalysts showed excellent selectivity for p-methoxybenzyl alcohol, converting it to the corresponding aldehyde through electro-oxidation with just 2.5 mol% of the electrocatalysts presented. The electrocatalysts maintained their excellent electroredox activity following recycling.

The electrochemical fabrication of electroactive polymer films from diamide- or diimide-cored N-phenylcarbazole dendrons for electrochromic applications

Hsiao, Sheng-Huei,Lin, Shu-Wei

, p. 1271 - 1280 (2016/02/18)

Two series of novel diamide- or diimide-cored N-phenylcarbazole dendrons were synthesized from condensation reactions of 3,6-di(carbazol-9-yl)-N-(4-aminophenyl)carbazole (NH2-3Cz) with aromatic dicarboxylic acids and tetracarboxylic dianhydrides, respectively. These dendrons can be electropolymerized into crosslinked poly(amide-carbazole) and poly(imide-carbazole) films on the electrode surface in an electrolyte solution via the coupling reactions between carbazole radical cations. Cyclic voltammograms of the electro-generated polymer films showed two reversible oxidation redox couples accompanied by a color change from the colorless neutral state to the yellow-green and blue oxidized forms in the range of 1.11-1.34 V. The electrochromic behavior of the film is clearly interpreted on the basis of spectroelectrochemical studies. Single layer electrochromic cells were also fabricated as preliminary evaluation for their application as electrochromic devices.

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