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1072-39-5

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1072-39-5 Usage

General Description

Erucic acid is a monounsaturated omega-9 fatty acid that is commonly found in certain plants, such as rapeseed and mustard seed. It is also present in small amounts in some animal fats, particularly in the fat of marine animals. Erucic acid has been associated with potential health risks, as higher levels of consumption have been linked to adverse effects on the heart, liver, and nervous system in some animal studies. Due to these concerns, erucic acid has been regulated in certain food products, particularly in oils and fats intended for human consumption. However, it is still used in various industrial applications, such as in the production of lubricants, plastics, and cosmetics.

Check Digit Verification of cas no

The CAS Registry Mumber 1072-39-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,7 and 2 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1072-39:
(6*1)+(5*0)+(4*7)+(3*2)+(2*3)+(1*9)=55
55 % 10 = 5
So 1072-39-5 is a valid CAS Registry Number.
InChI:InChI=1/C22H42O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22(23)24/h9-10H,2-8,11-21H2,1H3,(H,23,24)/b10-9-

1072-39-5SDS

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 13-Docosenoic acid

1.2 Other means of identification

Product number -
Other names brassylic acid

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:1072-39-5 SDS

1072-39-5Upstream product

1072-39-5Relevant 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 (2008/03/12)

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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