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

66287-29-4

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66287-29-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66287-29-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,2,8 and 7 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 66287-29:
(7*6)+(6*6)+(5*2)+(4*8)+(3*7)+(2*2)+(1*9)=154
154 % 10 = 4
So 66287-29-4 is a valid CAS Registry Number.

66287-29-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[(2,4-dichlorophenoxy)methyl]phenol

1.2 Other means of identification

Product number -
Other names 4-(2,4-dichlorophenoxy-methyl)-phenol

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:66287-29-4 SDS

66287-29-4Relevant academic research and scientific papers

REACTIVITY OF NEW PRECURSORS OF QUINONE METHIDES

Loubinoux, Bernard,Miazimbakana, Joseph,Gerardin, Philippe

, p. 1939 - 1942 (2007/10/02)

The azidomethylene protecting group allows the synthesis of unstable phenolic compounds which are used as quinone methide precursors in the alkylations of alcohols, phenols, azide, thiophenol, amines, enols and enolates.

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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