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Phenol, 2,6-dimethyl-4-[(4-methylphenyl)methyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

55563-86-5

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55563-86-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55563-86-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,5,6 and 3 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 55563-86:
(7*5)+(6*5)+(5*5)+(4*6)+(3*3)+(2*8)+(1*6)=145
145 % 10 = 5
So 55563-86-5 is a valid CAS Registry Number.

55563-86-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-dimethyl-4-[(4-methylphenyl)methyl]phenol

1.2 Other means of identification

Product number -
Other names 2,6,4'-Trimethyl-4-hydroxydiphenylmethan

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:55563-86-5 SDS

55563-86-5Downstream Products

55563-86-5Relevant academic research and scientific papers

Silica Gel as an Effective Catalyst for the Alkylation of Phenols and Some Heterocyclic Compounds

Kamitori, Yasuhiro,Hojo, Masaru,Masuda, Ryoichi,Izumi, Tatsuo,Tsukamoto, Shuichi

, p. 4161 - 4165 (2007/10/02)

In the presence of silica gel, the reaction of phenol with t-BuBr was examined under a variety of conditions and it was found that silica gel is an effective catalyst for the alkylation.As a result of this work 2-tert-butyl-, 2,6-di-tert-butyl-, and 2,4,6-tri-tert-butylphenols, all of which are hard to obtain directly by the Friedel-Crafts process, could be prepared easily by this one-step reaction.Several other alkyl halides were also used in this reaction.The alkylations of some heterocyclic aromatic compounds which cannot be alkylated by the conventional Friedel-Crafts method were also succesfully performed by this reaction.

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