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7289-47-6

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7289-47-6 Usage

Structure

Long-chain unsaturated hydrocarbon with 11 carbon atoms and a methoxy group attached to the first carbon

Usage

Intermediate in the synthesis of various organic compounds (e.g. fragrances, pharmaceuticals), starting material in the production of specialty chemicals, flavoring agent in the food industry

Physical properties

Colorless liquid, characteristic odor

Industrial applications

Wide range of uses as a starting material

Health and environmental risks

Low acute toxicity, low health and environmental risks when handled and used properly

Check Digit Verification of cas no

The CAS Registry Mumber 7289-47-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,8 and 9 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7289-47:
(6*7)+(5*2)+(4*8)+(3*9)+(2*4)+(1*7)=126
126 % 10 = 6
So 7289-47-6 is a valid CAS Registry Number.

7289-47-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 11-methoxyundec-1-ene

1.2 Other means of identification

Product number -
Other names 11-Methoxy-undec-1-en

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:7289-47-6 SDS

7289-47-6Relevant articles and documents

A new and highly effective organometallic approach to 1,2-dehalogenations and related reactions

Azzena, Ugo,Pittalis, Mario,Dettori, Giovanna,Pisano, Luisa,Azara, Emanuela

, p. 3892 - 3900 (2007)

We investigated the reductive elimination of several functionalized and non-functionalized vic-dibromides with 1,2-diphenyl-, 1,1,2,2-tetraphenyl- and 1-phenyl-2-(2-pyridyl)-1,2-disodioethane. The reaction, involving some of the less expensive organic and inorganic reagents, proceeds under mild conditions, and is tolerant of a variety of functional groups. Extension of this procedure to similar 1,2-disubstituted compounds was also investigated. Reductive eliminations run on stereochemical probe compounds strongly suggest that this reaction proceeds via a "single electron" reductive elimination reaction pathway.

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