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Carbonic acid, methoxymethyl 2-phenylethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

161529-95-9

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161529-95-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 161529-95-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,1,5,2 and 9 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 161529-95:
(8*1)+(7*6)+(6*1)+(5*5)+(4*2)+(3*9)+(2*9)+(1*5)=139
139 % 10 = 9
So 161529-95-9 is a valid CAS Registry Number.

161529-95-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2'-(methoxymethoxycarbonyloxy)ethylbenzene

1.2 Other means of identification

Product number -
Other names 2-(methoxymethoxycarbonyloxy)ethylbenzene

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:161529-95-9 SDS

161529-95-9Downstream Products

161529-95-9Relevant academic research and scientific papers

One-step synthesis of novel carbonates: Alkoxymethyl carbonates, from alcohols and chloromethyl alkyl ethers using silver carbonate

Teranishi,Nakao,Komoda,Hisamatsu,Yamada

, p. 176 - 180 (1995)

A synthesis of the novel carbonates, alkoxymethyl carbonates, is presented, starting with an alcohol. In the presence of silver carbonate, primary and secondary alcohols react with chloromethyl alkyl ethers in N,N-dimethylformamide under mild conditions to give the corresponding alkoxymethyl carbonates in good yields, without forming the alkoxymethyl ethers. The yields of alkoxymethyl carbonates are heavily influenced by the reaction solvent and this method is not applicable to tertiary alcohols. Methoxymethyl carbonate can be removed readily under mild basic or acidic conditions, and selective alkoxide interchange of the methoxymethoxide group occurs under basic conditions.

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