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3,3''-DIBROMO-4,4''-BIPHENOL is a chemical compound that belongs to the class of biphenols. It is composed of two phenol groups connected by a biphenyl bridge, with bromine atoms attached at the 3 and 3'' positions. 3,3''-DIBROMO-4,4''-BIPHENOL is known for its high thermal stability and effectiveness in reducing the flammability of materials.

189039-64-3

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189039-64-3 Usage

Uses

Used in Plastics Industry:
3,3''-DIBROMO-4,4''-BIPHENOL is used as a brominated flame retardant for plastics to enhance their fire resistance and safety.
Used in Textile Industry:
3,3''-DIBROMO-4,4''-BIPHENOL is used as a flame retardant in textiles to improve their fire safety and prevent rapid spread of flames in case of fire.
Used in Electronics Industry:
3,3''-DIBROMO-4,4''-BIPHENOL is used as a flame retardant in electronic components and devices to reduce the risk of fire and ensure safety.
However, it is important to note that 3,3''-DIBROMO-4,4''-BIPHENOL has been found to have potential environmental and health concerns, leading to restrictions on its use in some regions.

Check Digit Verification of cas no

The CAS Registry Mumber 189039-64-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,9,0,3 and 9 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 189039-64:
(8*1)+(7*8)+(6*9)+(5*0)+(4*3)+(3*9)+(2*6)+(1*4)=173
173 % 10 = 3
So 189039-64-3 is a valid CAS Registry Number.

189039-64-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-bromo-4-(2-bromo-4-hydroxyphenyl)phenol

1.2 Other means of identification

Product number -
Other names 3,3'-Dibromobiphenyl-4,4'-diol

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:189039-64-3 SDS

189039-64-3Upstream product

189039-64-3Relevant academic research and scientific papers

Synthesis and studies of the inhibitory effect of hydroxylated phenylpropanoids and biphenols derivatives on tyrosinase and laccase enzymes

Dettori, Maria Antonietta,Fabbri, Davide,Dessì, Alessandro,Dallocchio, Roberto,Carta, Paola,Honisch, Claudia,Ruzza, Paolo,Farina, Donatella,Migheli, Rossana,Serra, Pier Andrea,Pantaleoni, Roberto A.,Fois, Xenia,Rocchitta, Gaia,Delogu, Giovanna

, (2020/07/02)

The impaired activity of tyrosinase and laccase can provoke serious concerns in the life cycles of mammals, insects and microorganisms. Investigation of inhibitors of these two enzymes may lead to the discovery of whitening agents, medicinal products, anti-browning substances and compounds for controlling harmful insects and bacteria. A small collection of novel reversible tyrosinase and laccase inhibitors with a phenylpropanoid and hydroxylated biphenyl core was prepared using naturally occurring compounds and their activity was measured by spectrophotometric and electrochemical assays. Biosensors based on tyrosinase and laccase enzymes were constructed and used to detect the type of protein-ligand interaction and half maximal inhibitory concentration (IC50). Most of the inhibitors showed an IC50 in a range of 20–423 nM for tyrosinase and 23–2619 nM for laccase. Due to the safety concerns of conventional tyrosinase and laccase inhibitors, the viability of the new compounds was assayed on PC12 cells, four of which showed a viability of roughly 80% at 40 μM. In silico studies on the crystal structure of laccase enzyme identified a hydroxylated biphenyl bearing a prenylated chain as the lead structure, which activated strong and effective interactions at the active site of the enzyme. These data were confirmed by in vivo experiments performed on the insect model Tenebrio molitur.

Synthesis and thermal cyclopolymerization of heterocycle containing bis-ortho-diynyl arenes

Perera, K. Prasanna U.,Krawiec, Mariusz,Smith Jr., Dennis W.

, p. 10197 - 10203 (2007/10/03)

A new class of heteroatom terminated bis-ortho-diynyl arene (BODA) compounds have been synthesized via efficient in situ palladium catalyzed cross coupling between tetra alkynyl silanes and aryl bromides and iodides. BODA monomers undergo Bergman-type cyc

ETHYNYL SUBSTITUTED AROMATIC COMPOUNDS, SYNTHESIS, POLYMERS AND USES THEREOF

-

, (2008/06/13)

Compounds of ethynyl aromatic compounds form polymers which have high thermal stability. The monomers are useful for coating a wide variety of substances such as dielectric coatings where high thermal resistance is desirable including electronic components such as computer chips.

Ethynyl substituted aromatic compounds, synthesis, polymers and uses thereof

-

, (2008/06/13)

Compounds of ethynyl aromatic compounds form polymers which have high thermal stability. The monomers are useful for coating a wide variety of substances such as dielectric coatings where high thermal resistance is desirable including electronic components such as computer chips.

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