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Phenol, 4-[(4-methylphenoxy)methyl]-, also known as 4-(4-methylphenoxy)methylphenol or 4-(4-methylphenoxy)methylphenol, is an organic compound with the chemical formula C14H14O2. It is a derivative of phenol, where a 4-methylphenoxymethyl group is attached to the 4-position of the phenol ring. Phenol, 4-[(4-methylphenoxy)methyl]- is characterized by its aromatic structure, consisting of two phenyl rings connected through an ether linkage. It is a colorless to pale yellow solid with a molecular weight of 214.26 g/mol. This chemical is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals due to its unique reactivity and functional group presence.

953-13-9

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953-13-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 953-13-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,5 and 3 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 953-13:
(5*9)+(4*5)+(3*3)+(2*1)+(1*3)=79
79 % 10 = 9
So 953-13-9 is a valid CAS Registry Number.

953-13-9SDS

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 4-[(4-methylphenoxy)methyl]phenol

1.2 Other means of identification

Product number -
Other names Phenol,4-[(4-methylphenoxy)methyl]

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:953-13-9 SDS

953-13-9Relevant academic research and scientific papers

Practical process for the air oxidation of cresols: Part A. Mechanistic investigations

Barton, Benita,Logie, Catherine G.,Schoonees, Barbara M.,Zeelie, Bernard

, p. 62 - 69 (2012/12/24)

The catalytic air oxidation of p-cresol and 2,6-di-tert-butyl-4- methylphenol to the corresponding benzaldehydes was investigated to determine the mechanism at work in these oxidation reactions. A number of intermediates and byproducts, mainly in the form of dimers, were observed during the course of the reactions, and their structures were elucidated by spectroscopic and chromatographic methods. The existence of these compounds in the reaction mixtures, and their proposed methods of formation, provided further insight into the mechanism involved in these oxidations.

PROTECTION DES PHENOLS PAR LE GROUPEMENT AZIDOMETHYLENE APPLICATION A LA SYNTHESE DE PHENOLS INSTABLES

Loubinoux, Bernard,Tabbache, Samir,Gerardin, Philippe,Miazimbakana, Joseph

, p. 6055 - 6064 (2007/10/02)

Phenols are protected by the azidomethylene group in basic, nucleophilic, oxidative, weakly reductive and weakly acidic media.This group is obtained by the reaction of sodium azide with aryloxymethyl chlorides.Its utility lies in the ease with which it can be removed under very mild conditions which allows the synthesis of very unstable phenolic compounds.

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