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1,2-Benzenedicarbonitrile, 4-(4-aminophenoxy)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

189691-53-0

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189691-53-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 189691-53-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,9,6,9 and 1 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 189691-53:
(8*1)+(7*8)+(6*9)+(5*6)+(4*9)+(3*1)+(2*5)+(1*3)=200
200 % 10 = 0
So 189691-53-0 is a valid CAS Registry Number.

189691-53-0SDS

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 4-(4-aminophenoxy)benzene-1,2-dicarbonitrile

1.2 Other means of identification

Product number -
Other names 40aminophenoxyphthalonitrile

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:189691-53-0 SDS

189691-53-0Relevant academic research and scientific papers

Synthesis and characterization of bisphthalonitrile-terminated polyimide precursors with unique advantages in processing and adhesive properties

Li, Jianhui,Liu, Caizhao,Sun, Mingming,Xue, Gang,Zhang, Bin,Zhang, Xiwen,Zhang, Xugang,Zhou, Heng

, (2021)

The realization of the synthesis of melt-processable high-performance polyimide resin is of great interest. Herein, we prepared a new class of bisphthalonitrile functional bisimides used for polyimide precursors through 4,4′-bisphenol A dianhydride (BPADA

Characterization of electrodes modified with nanocomposites of cobalt tetraaminophenoxyphthalocyanine, reduced graphene and multi-walled carbon nanotubes

Shumba, Munyaradzi,Nyoni, Stephen,Britton, Jonathan,Nyokong, Tebello

, p. 1922 - 1935 (2019)

Glassy carbon electrodes or plates were modified with nanocomposites consisting of cobalt tetraaminophenoxyphthalocyanine (CoTAPhPc), reduced graphene oxide nanosheets (rGONs) and multi-walled carbon nanotubes (MWCNTs). The modified electrodes were charac

Synthesis and photophysical studies of CdTe quantum dot-monosubstituted zinc phthalocyanine conjugates

D'Souza, Sarah,Antunes, Edith,Nyokong, Tebello

, p. 173 - 181 (2011)

The linkage of unsymmetrically monosubstituted 4-aminophenoxy zinc phthalocyanine (ZnAPPc, 5) to CdTe quantum dots capped with mercaptopropionic acid (MPA), l-cysteine (l-cys) or thioglycolic acid (TGA) has been achieved using the coupling agents ethyl-N(

Adjustable magnetoresistance in semiconducting carbonized phthalonitrile resin

Du, Ai,Gao, Chong,Gu, Hongbo,Guo, Ying,Guo, Zhanhu,Shi, Zhong,Xie, Wenhao,Yang, Ming,Zhang, Hang,Zhou, Heng

, p. 9894 - 9897 (2021)

Herein, we report the first example of controllable magnetoresistance in a semiconducting carbonized phthalonitrile resin. This special phenomenon is explained using the different ratios of graphite-like (sp2) and diamond-like (sp3) bonds and localization

The substituted amino group type dependent sensitivity enhancing of cationic phthalocyanine derivatives for photodynamic activity

Lin, Dongmei,Wang, Yue,Zhang, Quanquan,Zhou, Jiahong,Zhou, Lin,Wei, Shaohua

, p. 107 - 120 (2016)

Many reports indicated that the cellular uptaken and photodynamic anti-cancer activity of amino group modified phthalocyanine (Pc) could be greatly improved in the acid environment around cancer cells because such Pc could transfer to their hydrochloride

Curing kinetics and thermal properties of imide containing phthalonitrile resin using aromatic amines

Choudhary, Veena,Kumar, Devendra

, (2020)

Due to their outstanding properties, phthalonitrile based polymers plays an important role in high performance advanced materials evaluated depending upon their curing process and mechanism. Henceforth it is necessary to understand the curing kinetics of

Low-melting phthalonitrile monomers containing maleimide group: Synthesis, dual-curing behavior, thermal and mechanical properties

Nechausov,Aleksanova,Morozov,Bulgakov,Babkin,Kepman

, (2021/05/27)

Novel dual-functional phthalonitrile monomers containing a maleimide group were synthesized and characterized. Ortho, meta, and para isomers were obtained and only the meta-isomer can be considered as a low melting phthalonitrile monomer with a melting po

Self-catalyzed resin monomer and synthesis method thereof

-

Paragraph 0021; 0037-0040, (2017/01/17)

The invention discloses a self-catalyzed resin monomer and a synthesis method thereof. The molecular structural formula of the self-catalyzed resin monomer is shown in the specification. The synthesis method includes the steps that 1, with p-aminophenol a

A multi-amine phthalocyanine and its derivatives, their preparation and use

-

Paragraph 0092-0094, (2017/03/08)

The invention discloses polyamine phthalocyanine and a derivative thereof. The structural general formula of the derivative of polyamine phthalocyanine is shown in descriptions. The derivative of polyamine phthalocyanine, disclosed by the invention, has r

Phthalocyanine-titanate nanotubes: A promising nanocarrier detectable by optical imaging in the so-called imaging window

Paris,Bernhard,Boudon,Heintz,Millot,Decrau

, p. 6315 - 6322 (2015/03/05)

TiONts-phthalocyanine nanohybrids combining an efficient optical probe and a promising nanovector have been developed in a step-by-step approach and were thoroughly characterized. Each 150 nm long TiONts-Pc bear ca. 450 Pc. Three nanohybrids were prepared including three different linkers in quest for the best stability.

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