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33486-90-7

33486-90-7

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33486-90-7 Usage

Chemical Properties

CLEAR COLOURLESS LIQUID

Synthesis Reference(s)

Synthetic Communications, 23, p. 749, 1993 DOI: 10.1080/00397919308009835

Check Digit Verification of cas no

The CAS Registry Mumber 33486-90-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,4,8 and 6 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 33486-90:
(7*3)+(6*3)+(5*4)+(4*8)+(3*6)+(2*9)+(1*0)=127
127 % 10 = 7
So 33486-90-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H8Cl2O/c1-11-5-6-7(9)3-2-4-8(6)10/h2-4H,5H2,1H3

33486-90-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-dichloro-2-(methoxymethyl)benzene

1.2 Other means of identification

Product number -
Other names 2,6-Dichlorobenzyl Methyl 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:33486-90-7 SDS

33486-90-7Relevant articles and documents

A convenient synthesis of methyl- and isopropyl-benzyl ethers using silver(II) oxide as reagent

Ortiz,Walls,Yuste,Barrios,Sanchez-Obregon,Pinelo

, p. 749 - 756 (2007/10/02)

Substituted bromomethyl- and chloromethylbenzenes and bis(bromomethyl) benzenes were directly converted, in high yields, to the corresponding methyl- and isopropyl-benzyl ethers by treatment with silver(II) oxide in methanol or isopropanol.

Unusual O-Alkylation with Iodomethyltrimethylsilane

Chakraborty, T. K.,Reddy, G. V.

, p. 251 - 253 (2007/10/02)

Iodomethyltrimethylsilane alkylates alkoxide ions giving rise to O-methyl and O-trimethylsilyl ethers which are formed by cleavage of the silicon-carbon bond.

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