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115319-74-9

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115319-74-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 115319-74-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,3,1 and 9 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 115319-74:
(8*1)+(7*1)+(6*5)+(5*3)+(4*1)+(3*9)+(2*7)+(1*4)=109
109 % 10 = 9
So 115319-74-9 is a valid CAS Registry Number.

115319-74-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-hydroxybenzyl 2-(2-methoxyethoxy)ethyl ether

1.2 Other means of identification

Product number -
Other names 4-{2-(2-methoxyethoxy)ethoxymethyl}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:115319-74-9 SDS

115319-74-9Downstream Products

115319-74-9Relevant articles and documents

Compounds and methods of arylmethylation (benzylation) as protection for alcohol groups during chemical synthesis

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Page/Page column 4-5; 10, (2010/07/14)

A process for benzylating an alcohol includes mixing 2-benzyloxy-1-methylpyridinium triflate in an aromatic hydrocarbon solvent having a predetermined boiling point; adding an acid scavenger to the mixture; combining the alcohol to be benzylated with the mixture; reacting the alcohol with the 2-benzyloxy-1-methylpyridinium triflate by heating above ambient temperature to generate the benzylated alcohol; and separating the benzylated alcohol from the mixture.

ON THE METALATION OF PHENOLIC COMPOUNDS: READY ACCESS TO HIGHLY SUBSTITUTED PHENOLS.

Costa, Antonio,Saa, Jose M.

, p. 5551 - 5554 (2007/10/02)

The direct metalation of several p-hydroxybenzylmethyl ethers has been studied.Those substrates possesing an electron-withdrawing group in a 1,3 relationship with the coordinating (-CH2OMe) group underwent regioselective metalation by the action of n-BuLi/THF.Highly substituted phenols can thus be readily prepared.

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