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(2-Methoxyethyl)cyclohexane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

51284-32-3

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51284-32-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51284-32-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,2,8 and 4 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 51284-32:
(7*5)+(6*1)+(5*2)+(4*8)+(3*4)+(2*3)+(1*2)=103
103 % 10 = 3
So 51284-32-3 is a valid CAS Registry Number.

51284-32-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-methoxyethyl)cyclohexane

1.2 Other means of identification

Product number -
Other names (2-Methoxy-ethyl)-cyclohexane

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:51284-32-3 SDS

51284-32-3Downstream Products

51284-32-3Relevant academic research and scientific papers

Synthesis of ethers from esters via Fe-catalyzed hydrosilylation

Das, Shoubhik,Li, Yuehui,Junge, Kathrin,Beller, Matthias

supporting information, p. 10742 - 10744 (2013/01/15)

Triiron dodecacarbonyl allows for the selective reduction of esters into the corresponding ethers. This protocol has a wide substrate scope. In addition, cholesteryl pelarogonate has been reduced under the reaction conditions with an excellent yield.

Hexafluoroisopropanol: A powerful solvent for the hydrogenation of functionalized aromatic compounds

Fache, Fabienne,Piva, Olivier

, p. 1294 - 1296 (2007/10/03)

Various substituted aromatic compounds have been reduced under H 2 using RuCl3. The fluorous solvent hexafluoroisopropanol turned out to be particularly efficient in the case of compounds difficult to reduce in organic solvents.

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