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1,3-Benzenedicarboxylic acid, 4,6-dibromo-, dimethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

90766-77-1

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90766-77-1 Usage

Usage

Flame retardant in plastics and textiles

Effectiveness

Highly effective at preventing the spread of fires

Environmental Impact

Potential environmental pollutant

Persistence

Persists in the environment

Bioaccumulation

Accumulates in organisms

Health Risks

Potential health risks due to exposure

Concerns

Growing concern about its use due to health and environmental risks

Alternatives

Efforts being made to find safer alternatives for flame retardant applications

Check Digit Verification of cas no

The CAS Registry Mumber 90766-77-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,7,6 and 6 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 90766-77:
(7*9)+(6*0)+(5*7)+(4*6)+(3*6)+(2*7)+(1*7)=161
161 % 10 = 1
So 90766-77-1 is a valid CAS Registry Number.

90766-77-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name dimethyl 4,6-dibromobenzene-1,3-dicarboxylate

1.2 Other means of identification

Product number -
Other names 4,6-Dibrom-isophthalsaeure-dimethylester

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:90766-77-1 SDS

90766-77-1Relevant academic research and scientific papers

Diazapentacenes from Quinacridones

Wiesner, Thomas,Ahrens, Lukas,Rominger, Frank,Freudenberg, Jan,Bunz, Uwe H. F.

, p. 4553 - 4556 (2021/02/26)

Bis(silylethynylated) 5,7- and 5,12-diazapentacenes were synthesized from cis- and trans-quinacridone using protection, alkynylation and deoxygenation. The solid-state packing of the targets is determined by choice and position of the silylethynyl substit

Singlet Biradical Versus Triplet Biradical/Zwitterion Characteristics in Isomers of C6?C5?C6?C7?C6-Fused Pentacyclic Aromatic Hydrocarbons Revealed through Reactivity Patterns

Zhen, Cian-Jhe,Lu, Shu-Feng,Lin, Min-Hwa,Wu, Jay-Tai,Chao, Ito,Lin, Chih-Hsiu

, p. 16682 - 16689 (2021/11/01)

Among various polycyclic aromatic hydrocarbons, C6?C5?C6?C7?C6 fused pentacyclic aromatic hydrocarbons have the unique potential to adopt quinonoid, zwitterion, singlet, or triplet biradical electroni

Luminescent Anion Sensing by Transition-Metal Dipyridylbenzene Complexes Incorporated into Acyclic, Macrocyclic and Interlocked Hosts

Beer, Paul D.,Dapin, Sophie,Knighton, Richard C.

, p. 5288 - 5296 (2020/04/24)

A series of novel acyclic, macrocyclic and mechanically interlocked luminescent anion sensors have been prepared by incorporation of the isophthalamide motif into dipyridylbenzene to obtain cyclometallated complexes of platinum(II) and ruthenium(II). Both

Synthesis and properties of novel N,C,N terdentate skeleton based on 1,3-di(pyridin-2-yl)benzene moiety—new tricks for old dogs

Tan, Shuai,Wu, Xiugang,Zheng, Yanqiong,Wang, Yafei

, p. 1951 - 1954 (2019/09/12)

Utilization of intermolecular Friedel–Crafts and intramolecular condensation reaction, novel 1,3-di(pyridine-2-yl)benzene(N,C,N terdentate) skeleton with electro-withdrawing group in 6' position of pyridyl and a cyclization between 6' position of pyridyl and 6 position of benzyl ring were firstly designed and synthesized. The structures of these novel N,C,N terdentate were confirmed by NMR, MS and X-ray single crystalanalyses. The photophysical properties of these compounds were briefly explored.

Highly active catalysts for the transfer dehydrogenation of alkanes: Synthesis and application of novel 7-6-7 ring-based pincer iridium complexes

Shi, Yuan,Suguri, Takuya,Dohi, Chisato,Yamada, Hirotsuna,Kojima, Satoshi,Yamamoto, Yohsuke

, p. 10672 - 10689 (2013/08/23)

A series of Ir-PCP pincer precatalysts [(7-6-7-RPCP)Ir(H)(Cl)] and [(7-6-7-ArPCP)Ir(H)(Cl)(MeCN)] bearing a novel "7-6-7" fused-ring skeleton have been synthesized based upon the postulate that the catalytic species would have durability due to their rather rigid structure and high activity owing to the low but sufficient flexibility of their backbones, which are not completely fixed. Treatment of these precatalysts with NaOtBu gave rise to the active 14 electron (14e) species [(7-6-7-iPrPCP)Ir] and [(7-6-7-PhPCP)Ir], which can trap hydrogen and were spectroscopically characterized as the tetrahydride complexes. Both [(7-6-7-iPrPCP)Ir] and [(7-6-7-PhPCP)Ir] were found to be highly effective in the transfer dehydrogenation of cyclooctane with tert-butylethylene as the hydrogen acceptor, the initial reaction rate at high temperature (230°C) being higher for [(7-6-7-iPrPCP)Ir] than [(7-6-7-PhPCP)Ir], and the turnover number (TON) of the overall hydrogen transfer being higher for the latter. Nonetheless, the estimated TONs were as high as 4600 and 4820 for the two complexes at this temperature, respectively, which are unprecedented absolute values. In terms of durability, the [(7-6-7-PhPCP)Ir] complex is the catalyst of choice for this reaction. Structural analysis and computational studies support the importance of the low flexibility of the ligand core. Copyright

Ladder oligo(m -aniline)s: Derivatives of azaacenes with cross-conjugated π-systems

Rajca, Andrzej,Boratynski, Przemyslaw J.,Olankitwanit, Arnon,Shiraishi, Kouichi,Pink, Maren,Rajca, Suchada

, p. 2107 - 2120 (2012/05/20)

We describe the synthesis and electronic properties of ladder oligomers of poly(m-aniline) that may be considered as derivatives of azaacenes with cross-conjugated π-systems. Syntheses of ladder oligo(m-aniline)s with 9 and 13 collinearly fused six-member

Conformationally constrained, stable, triplet ground state (S = 1) nitroxide diradicals. Antiferromagnetic chains of S = 1 diradicals

Rajca, Andrzej,Takahashi, Masahiro,Pink, Maren,Spagnol, Gaelle,Rajca, Suchada

, p. 10159 - 10170 (2008/03/11)

Nitroxide diradicals, in which nitroxides are annelated to m-phenylene forming tricyclic benzo-bisoxazine-like structures, have been synthesized and characterized by X-ray crystallography, magnetic resonance (EPR and 1H NMR) spectroscopy, as we

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