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57792-42-4

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57792-42-4 Usage

General Description

1-(hexadecyloxy)-4-methylbenzene, also known as 4-methylhexadecylanisole, is a chemical compound that belongs to the family of benzene derivatives. It is a white crystalline solid with a molecular formula of C23H38O and a molecular weight of 330.55 g/mol. This chemical is commonly used as an intermediate in the synthesis of various pharmaceuticals, cosmetics, and fragrances. It is also used as a flavoring agent in food products. Additionally, 1-(hexadecyloxy)-4-methylbenzene has been shown to exhibit antioxidant and antifungal properties, making it potentially valuable in a variety of industrial and commercial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 57792-42-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,7,9 and 2 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 57792-42:
(7*5)+(6*7)+(5*7)+(4*9)+(3*2)+(2*4)+(1*2)=164
164 % 10 = 4
So 57792-42-4 is a valid CAS Registry Number.

57792-42-4SDS

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-hexadecoxy-4-methylbenzene

1.2 Other means of identification

Product number -
Other names hexadecyl-p-tolyl 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:57792-42-4 SDS

57792-42-4Relevant articles and documents

Alkoxylated p-phenylenevinylene oligomers: Synthesis and spectroscopic and electrochemical properties

Ndayikengurukiye, Henri,Jacobs, Sven,Tachelet, Wim,Van Der Looy, Johan,Pollaris, Anne,Geise, Herman J.,Claeys, Magda,Kauffmann, Jean M.,Janietz, Silvia

, p. 13811 - 13828 (2007/10/03)

Twenty-one n-alkoxy substituted phenylenevinylene oligomers were synthesized, varying in size, number and position of the OR groups. IR,MS and solubility data are presented. NMR measurements provided the molecular structure as well as information about conformations and molecular dynamics. UV and of cyclic voltammetric data give correlations of chemical structure (number and position of OR substituents) with separate HOMO and LUMO energies.

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