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M-BIS(M-PHENOXYPHENOXY)BENZENE, also known as 2,2'-[1,4-phenylenebis(oxy)]bis[4-phenoxyphenol], is a chemical compound with the molecular formula C30H24O2. It is a versatile building block in the synthesis of various polymers and materials, known for its high thermal stability, flame retardant properties, and potential antioxidant and antimicrobial properties.

2455-71-2

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2455-71-2 Usage

Uses

Used in Polymer Synthesis:
M-BIS(M-PHENOXYPHENOXY)BENZENE is used as a building block for synthesizing various polymers, such as poly(arylene ether ketone) and poly(arylene ether sulfone). Its incorporation enhances the thermal stability and flame retardant properties of these polymers, making them suitable for high-performance applications.
Used in Liquid Crystal Material Production:
M-BIS(M-PHENOXYPHENOXY)BENZENE is used as a reactant in the production of liquid crystal materials. Its unique molecular structure contributes to the formation of liquid crystal phases, which are essential for display and optical applications.
Used in Adhesives and Coatings:
M-BIS(M-PHENOXYPHENOXY)BENZENE is used as a component in adhesives and coatings. Its high thermal stability and flame retardant properties make it an ideal additive for improving the performance of these materials in various industrial applications.
Used in Medical and Healthcare Applications:
Due to its potential antioxidant and antimicrobial properties, M-BIS(M-PHENOXYPHENOXY)BENZENE may find use in certain medical and healthcare applications, such as in the development of antimicrobial coatings or as an antioxidant agent in pharmaceutical formulations.
Used in Flame Retardant Applications:
M-BIS(M-PHENOXYPHENOXY)BENZENE is used as a flame retardant in various industries, including plastics, textiles, and electronics. Its high thermal stability and flame retardant properties make it an effective additive for improving the fire safety of these materials.
Used in High-Performance Materials:
M-BIS(M-PHENOXYPHENOXY)BENZENE is used in the development of high-performance materials for applications that require excellent thermal stability and flame resistance, such as aerospace, automotive, and electrical industries.

Check Digit Verification of cas no

The CAS Registry Mumber 2455-71-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,5 and 5 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2455-71:
(6*2)+(5*4)+(4*5)+(3*5)+(2*7)+(1*1)=82
82 % 10 = 2
So 2455-71-2 is a valid CAS Registry Number.
InChI:InChI=1/C30H22O4/c1-3-10-23(11-4-1)31-25-14-7-16-27(20-25)33-29-18-9-19-30(22-29)34-28-17-8-15-26(21-28)32-24-12-5-2-6-13-24/h1-22H

2455-71-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-bis(3-phenoxyphenoxy)benzene

1.2 Other means of identification

Product number -
Other names m-Bis(m-phenoxyphenoxy)benzene

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:2455-71-2 SDS

2455-71-2Relevant academic research and scientific papers

Sonocatalytic degradation of a textile dye over Gd-doped ZnO nanoparticles synthesized through sonochemical process

Khataee, Alireza,Soltani, Reza Darvishi Cheshmeh,Karimi, Atefeh,Joo, Sang Woo

, p. 219 - 230 (2015/02/19)

The present study was performed to sonochemically synthesize GdxZn1-xO (x = 0-0.1) nanoparticles for sonocatalysis of Acid Orange 7 (AO7) in an aqueous medium. The results of X-ray diffraction (XRD), scanning electron microscopy (SEM

FLAME RETARDANT HALOGENATED PHENYL ETHERS

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Page/Page column 13, (2011/08/08)

A halogenated non-polymeric phenyl ether is described having the general formula (I): wherein each X is independently Cl or Br, n is an integer of 1 or 2, each m is independently an integer of 1 to 5 and each p is independently an integer of 1 to 4, provided that, when X is Cl, the total amount halogen in the ether is from about 50 to about 65 wt% and when, X is Br, the total amount halogen in the ether is from at least 70 wt % to about 79 wt%.

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