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Benzene, [[(1-methylethoxy)methoxy]methyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

91968-51-3

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91968-51-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91968-51-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,9,6 and 8 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 91968-51:
(7*9)+(6*1)+(5*9)+(4*6)+(3*8)+(2*5)+(1*1)=173
173 % 10 = 3
So 91968-51-3 is a valid CAS Registry Number.

91968-51-3SDS

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 propan-2-yloxymethoxymethylbenzene

1.2 Other means of identification

Product number -
Other names Isopropyloxymethyl-benzyl-aether

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:91968-51-3 SDS

91968-51-3Downstream Products

91968-51-3Relevant academic research and scientific papers

Efficient and selective formation of mixed acetals by Nafion-H SAC-13 silica nanocomposite solid acid catalyst

Ledneczki, Istvan,Molnar, Arpad

, p. 3683 - 3690 (2007/10/03)

Various types of hydroxy compounds can readily be converted to the corresponding mixed acetals with dialkoxymethanes in the presence of SAC-13 solid superacid. The transformation is almost instantaneous, product acetals are isolated in good to excellent yields, and the catalyst can be reused with minor loss of activity. Comparative studies were also carried out with p-toluenesulfonic acid and BF3·OEt2.

Enantiotopic group differentiation and kinetic resolution: Asymmetric reduction of meso-1,3-dihalides

Michael Chong,Sokoll, Kenneth K.

, p. 879 - 882 (2007/10/02)

Asymmetric reduction of 1,3-dihalides derived from glycerol occurs with moderate levels of enantiotopic group differentiation. A concomitant kinetic resolution increases the enantiometric purity of the initial product.

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