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3,3'-Dibromodiphenyl Ether is a chemical compound that belongs to the class of brominated flame retardants. It is characterized by the presence of two bromine atoms attached to a diphenyl ether structure. 3,3?DIBROMODIPHENYL ETHER is known for its ability to contaminate foods and dietary products, raising concerns about its potential health and environmental impacts.

6903-63-5

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6903-63-5 Usage

Uses

Used in Flame Retardant Industry:
3,3'-Dibromodiphenyl Ether is used as a flame retardant additive in various materials, such as plastics, textiles, and electronics, to reduce the risk of fire and improve their fire resistance. Its application in this industry is primarily due to its ability to slow down the spread of flames and reduce the heat release rate during combustion.
Used in Food and Dietary Products:
Unfortunately, 3,3'-Dibromodiphenyl Ether has been found to contaminate foods and dietary products, which can pose potential health risks to consumers. The presence of this chemical in the food supply chain is a concern that needs to be addressed through proper regulation and monitoring to ensure the safety and quality of food products.

Check Digit Verification of cas no

The CAS Registry Mumber 6903-63-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,0 and 3 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6903-63:
(6*6)+(5*9)+(4*0)+(3*3)+(2*6)+(1*3)=105
105 % 10 = 5
So 6903-63-5 is a valid CAS Registry Number.

6903-63-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-bromo-3-(3-bromophenoxy)benzene

1.2 Other means of identification

Product number -
Other names m,m'-Dibromdiphenylether

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:6903-63-5 SDS

6903-63-5Relevant academic research and scientific papers

Iptycene pyridazine tetradentate platinum complex phosphorescent material, preparation method and application thereof

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Paragraph 0057-0059, (2020/03/16)

The invention discloses an iptycene pyridazine tetradentate platinum complex phosphorescent material, a preparation method and application thereof. The oxygen atom bridged pyridazine tetradentate platinum complex based on iptycene modification has a struc

Ptycene pyridazine octadentate diplatinum complex phosphorescent material as well as preparation method and application thereof

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Paragraph 0010; 0052-0054, (2020/07/14)

The invention discloses a ptycene pyridazine octadentate diplatinum complex phosphorescent material as well as a preparation method and application thereof. The invention relates to a ptycene-modifiedpyridazine octadentate diplatinum complex bridged by oxygen atoms. According to a phosphorescent platinum complex disclosed by the invention, binuclear platinum is introduced into a rigid non-conjugated ptycene ligand, so that the light-emitting center is increased while the light-emitting efficiency reduction caused by a pi-pi accumulation effect is inhibited, and the light-emitting color of theplatinum complex phosphorescent material is adjusted to a great extent. Compared with mononuclear platinum complexes with the same light-emitting color, the obtained ptycene-modified pyridazine diplatinum complex has higher light-emitting efficiency, light-emitting brightness and thermal stability. According to an electroluminescent device provided by the invention, the light-emitting layer is prepared by adopting a spin-coating film preparation method under specific conditions, so that the cost is low, the operation is simple, the chemical property is stable, the light-emitting brightness and efficiency are high, and the realization of an efficient electroluminescent device is facilitated.

ORGANOMETALLIC COMPOUND, ORGANIC LIGHT-EMITTING DEVICE INCLUDING THE ORGANOMETALLIC COMPOUND, AND DIAGNOSTIC COMPOSITION INCLUDING THE ORGANOMETALLIC COMPOUND

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Paragraph 0331; 0336; 0337; 0344; 0345; 0346, (2019/07/10)

An organometallic compound represented by Formula 1: wherein, in Formula 1, groups and variables are the same as described in the specification.

BLUE AND NARROW BAND GREEN AND RED EMITTING METAL COMPLEXES

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Paragraph 0088; 0089, (2019/09/20)

The present invention includes tetradentate platinum (II) complexes for narrow band green and red phosphorescent emitters. The present invention also includes blue emitting metal complexes with six-membered chelate rings based on fused carbazole. The pres

Selective one-pot access to symmetrical or unsymmetrical diaryl ethers by copper-catalyzed double arylation of a simple oxygen source

Tlili, Anis,Monnier, Florian,Taillefer, Marc

supporting information; experimental part, p. 12299 - 12302 (2011/02/16)

Great CO-mbination: A novel method is reported for the controlled one-pot synthesis of various symmetrical or unsymmetrical diaryl ethers by double arylation of a simple inorganic oxygen source (see scheme). This versatile and highly selective process is based on the use of a cheap and low toxicity copper catalytic system.

Synthesis and Characterization of Polybrominated Diphenyl Ethers - Unlabelled and Radiolabelled Tetra,- Penta- and Hexa-bromodiphenyl Ethers

Oern, Ulrika,Eriksson, Lars,Jakobsson, Eva,Bergman, Ake

, p. 802 - 807 (2007/10/03)

Diphenyl ether, 3-bromodiphenyl ether and 3,3'-dibromodiphenyl ether have been synthesized via coupling of the appropriate phenol and bromobenzene.Each of these compounds was subsequently brominated to (i) 2,2',4,4'-tetrabromodiphenyl ether, (ii) 2,2'3,4,

Brominated Diphenyl Ethers - an Important Step on the Way to Synthetic Lubricants

Kreisel, Guenter,Rudolph, Gundula,Schulze, Dieter Karl-Wilhelm,Poppitz, Wolfgang

, p. 1153 - 1162 (2007/10/02)

The described synthesis of synthetic lubricants based on polyphenyl ethers requires an analytical characterization of the isomerization step, which is important to the process optimization.The separation of the intermediates succeeds with gas chromatography; the isomers are determined using a retention index system.The obtained results are compared with the composition of the final product, which was investigated by HPLC analysis.Keywords.Gas chromatography; Polyphenyl ethers; Lubricants, synthetic.

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