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Benzene, 1-ethoxy-4-(methoxymethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

103441-19-6

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103441-19-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 103441-19-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,4,4 and 1 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 103441-19:
(8*1)+(7*0)+(6*3)+(5*4)+(4*4)+(3*1)+(2*1)+(1*9)=76
76 % 10 = 6
So 103441-19-6 is a valid CAS Registry Number.

103441-19-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-ethoxy-4-(methoxymethyl)benzene

1.2 Other means of identification

Product number -
Other names 1-ethoxy-4-methoxymethyl-benzene

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:103441-19-6 SDS

103441-19-6Downstream Products

103441-19-6Relevant academic research and scientific papers

Direct synthesis of ethers from aldehydes and ketones. One-pot reductive etherification of benzaldehydes, alkyl aryl ketones, and benzophenones

Mochalov,Fedotov,Trofimova,Zefirov

, p. 503 - 512 (2016/06/13)

Benzyl alcohols formed by the reduction of benzaldehydes, alkyl aryl ketones, and benzophenones with sodium tetrahydridoborate in alcohols undergo in situ etherification with the solvent in the presence of a catalytic amount of HCl. Thus the process may be regarded as one-pot transformation of carbonyl compounds into the corresponding benzyl ethers. The yields of ethers depend on the substituent nature in the aromatic fragment of the initial carbonyl compound and on the alcohol used as reduction medium.

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