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954374-43-7

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  • Factory Price OLED 99% 954374-43-7 4,5,9,10-tetrabromo-2,7-dioctylbenzo[lmn][3,8] phenanthroline-1,3,6,8-tetraone Manufacturer

    Cas No: 954374-43-7

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954374-43-7 Usage

General Description

4,5,9,10-Tetrabromo-2,7-dioctylbenzo[lMn][3,8]phenanthroline-1,3,6,8-tetraone is a chemical compound with the molecular formula C56H56Br4N2O4. It is a complex organic compound that contains bromine and nitrogen atoms as well as a benzo[lMn][3,8]phenanthroline backbone. 4,5,9,10-TetrabroMo-2,7-dioctylbenzo[lMn][3,8]phenanthroline-1,3,6,8-tetraone is characterized by its high molecular weight and its potential use as a metal-ligand complex in various chemical reactions. It is also known for its potential applications in materials science, organic chemistry, and pharmaceutical research. However, due to its complex structure and potentially hazardous nature, this compound requires careful handling and storage.

Check Digit Verification of cas no

The CAS Registry Mumber 954374-43-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,4,3,7 and 4 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 954374-43:
(8*9)+(7*5)+(6*4)+(5*3)+(4*7)+(3*4)+(2*4)+(1*3)=197
197 % 10 = 7
So 954374-43-7 is a valid CAS Registry Number.

954374-43-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,5,9,10-Tetrabromo-2,7-dioctylbenzo[lmn][3,8]phenanthroline-1,3,6,8(2H,7H)-tetraone

1.2 Other means of identification

Product number -
Other names -

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:954374-43-7 SDS

954374-43-7Relevant articles and documents

A near-infrared fluoride sensor based on a substituted naphthalenediimide-anthraquinone conjugate

Bobe, Sharad R.,Bhosale, Sidhanath V.,Jones, Lathe,Puyad, Avinash L.,Raynor, Aaron M.,Bhosale, Sheshanath V.

, p. 4762 - 4766 (2015)

The synthesis and characterization of a highly selective fluoride receptor based on a naphthalene diimide substituted with an anthraquinone (NDI-AQ) moiety is described. In CHCl3, the receptor was shown to be highly selective for fluoride (Ka~103 M-1) over other anions (AcO-, HSO4-, Br-, Cl-, I-, ClO4-, H2PO4-, and NO3-) with pronounced changes in absorption characteristics, that is, red-shift of the absorption band to 790 nm (NIR). The visual color change, NIR shift in absorption, emission spectroscopy, and electrochemistry thus support an intramolecular charge transfer (ICT) effect upon fluoride binding to the NDI-AQ receptor.

First synthesis of 2,3,6,7-tetrabromonaphthalene diimide

Gao, Xike,Qiu, Wenfeng,Yang, Xiaodi,Liu, Yunqi,Wang, Ying,Zhang, Hengjun,Qi, Ting,Liu, Ying,Lu, Kun,Du, Chunyan,Shuai, Zhigang,Yu, Gui,Zhu, Daoben

, p. 3917 - 3920 (2007)

N,N′-Bis(n-octyl)-2,3,6,7-tetrabromonaphthalene diimide (TBNDI) was synthesized by a new imidization reaction and characterized by HRMS, 1H NMR, 13C NMR, elemental analyses, FT-IR, UV-vis, and single-crystal X-ray analysis. The TBNDIs are the key precursors for the synthesis of core-tetrasubstituted-naphthalene diimides.

Core-fluorinated naphthalene diimides: Synthesis, characterization, and application in n-type organic field-effect transistors

Yuan, Zhongyi,Ma, Yingjie,Ge?ner, Thomas,Li, Mengmeng,Chen, Long,Eustachi, Michael,Weitz, R. Thomas,Li, Chen,Müllen, Klaus

supporting information, p. 456 - 459 (2016/02/18)

A series of difluoro- and tetrafluoro-substituted naphthalene diimides (NDIs) were synthesized by halogen exchange reactions of corresponding bromo-NDIs with CsF in dioxane. Two strong electron acceptor molecules 6 and 8 with low-lying LUMO energy levels of -4.27 and -4.54 eV were obtained, starting from tetrafluoro-NDI. Organic field-effect transistors (OFETs) based on these fluorinated NDIs were fabricated by vapor deposition, exhibiting n-channel field-effect character under ambient conditions with the highest mobility of 0.1 cm2 V-1 s-1.

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