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1-methyl-2-{[(E)-2-phenylethenyl]oxy}benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

32546-86-4

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32546-86-4 Usage

Molecular Structure

Consists of a benzene ring and a methyl group.

Ether Bond

Contains a 2-phenylethenyl molecule attached to the benzene ring.

Organic Synthesis

Frequently used in the synthesis of various aromatic compounds and derivatives.

Research Utility

Valuable tool for chemists and researchers in studying and developing new chemical compounds.

Unique Properties

Its specific structure and properties make it a useful compound in chemical research.

Check Digit Verification of cas no

The CAS Registry Mumber 32546-86-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,5,4 and 6 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 32546-86:
(7*3)+(6*2)+(5*5)+(4*4)+(3*6)+(2*8)+(1*6)=114
114 % 10 = 4
So 32546-86-4 is a valid CAS Registry Number.

32546-86-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methyl-2-[(E)-2-phenylethenoxy]benzene

1.2 Other means of identification

Product number -
Other names -

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:32546-86-4 SDS

32546-86-4Downstream Products

32546-86-4Relevant academic research and scientific papers

Vinyl aryl ethers from copper-catalyzed coupling of vinyl halides and phenols

Wan, Zhonghui,Jones, Chauncey D.,Koenig, Thomas M.,Pu, Y. John,Mitchell, David

, p. 8257 - 8259 (2003)

A general procedure for vinyl aryl ether bond formation by direct coupling of vinyl halides and phenols under mild Ullmann-type reaction conditions has been developed. Using copper chloride as the catalyst and cesium carbonate as the base, vinyl bromides or iodides were reacted with phenols in refluxing toluene to produce vinyl aryl ethers in good to excellent yields.

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