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4542-75-0

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4542-75-0 Usage

General Description

4,4'-Bis(bromomethyl)-diphenyl ether is a chemical compound consisting of two phenyl rings connected by an oxygen atom, with bromomethyl groups attached to each phenyl ring. It is commonly used as a flame retardant in a variety of plastic and resin products, as well as in electrical and electronic equipment. 4,4'-BIS(BROMOMETHYL)-DIPHENYL ETHER is known for its high thermal stability and ability to inhibit the spread of flames by releasing bromine radicals during combustion. However, concerns have been raised about the potential health and environmental impacts of 4,4'-bis(bromomethyl)-diphenyl ether, leading to some regulatory restrictions on its use in certain regions.

Check Digit Verification of cas no

The CAS Registry Mumber 4542-75-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,5,4 and 2 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4542-75:
(6*4)+(5*5)+(4*4)+(3*2)+(2*7)+(1*5)=90
90 % 10 = 0
So 4542-75-0 is a valid CAS Registry Number.
InChI:InChI=1/C14H12Br2O/c15-9-11-1-5-13(6-2-11)17-14-7-3-12(10-16)4-8-14/h1-8H,9-10H2

4542-75-0SDS

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 1-(bromomethyl)-4-[4-(bromomethyl)phenoxy]benzene

1.2 Other means of identification

Product number -
Other names di-p-(bromomethyl)phenyl ether

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:4542-75-0 SDS

4542-75-0Relevant articles and documents

Synthesis of bis-4H-furo[3,4-b]indoles

McGowan, Meredeth A.,Perreault, Denise M.,Thornton, Nancy B.,Garaas, Sarah D.,Gribble, Gordon W.

, p. 334 - 347 (2018/09/10)

We describe the synthesis of two novel bis-4H-furo[3,4-b]indoles from indole. Several alternative pathways to these potential DNA bis-intercalator precursors are discussed, and the synthesis of a novel semi-rigid tether is reported.

Rotaxanes from tetralactams

Gibson, Harry W.,Wang, Hong,Niu, Zhenbin,Slebodnick, Carla,Zhakharov, Lev N.,Rheingold, Arnold L.

experimental part, p. 1270 - 1280 (2012/06/18)

Attempts to incorporate a tetralactam (3a) into a side-chain polyrotaxane by formation of its complex with p-tritylphenolate and reaction with poly(vinybenzyl chloride) failed, probably due to steric hindrance. However, three new small molecule model rota

Strong binding of alkylguanidinium ions by molecular tweezers: An artificial selective arginine receptor molecule with a biomimetic recognition pattern

Schrader, Thomas

, p. 1537 - 1541 (2007/10/03)

Bisphosphonates 2 and 3 represent the first artificial receptor molecules for alkylguanidinium ions. They bind to the guanidinium moiety by forming a 1:l chelate complex, stabilized by a planar network of electrostatic interactions and hydrogen bonds. Thi

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