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128389-74-2

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128389-74-2 Usage

General Description

1,3-DIERUCIN is a chemical compound that belongs to the class of lignans, which are organic compounds found in various plants. It is specifically found in the seeds of the Chinese herbal medicine known as Fructus Schisandrae, and has been studied for its potential pharmacological and medicinal properties. Research has shown that 1,3-DIERUCIN has antioxidant, anti-inflammatory, and neuroprotective effects, making it a potentially valuable compound for the development of natural remedies and pharmaceuticals. Additionally, it has been found to modulate the immune response and exhibit anti-cancer activity, making it a promising candidate for further research in the fields of medicine and human health.

Check Digit Verification of cas no

The CAS Registry Mumber 128389-74-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,3,8 and 9 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 128389-74:
(8*1)+(7*2)+(6*8)+(5*3)+(4*8)+(3*9)+(2*7)+(1*4)=162
162 % 10 = 2
So 128389-74-2 is a valid CAS Registry Number.

128389-74-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name [3-[(Z)-docos-13-enoyl]oxy-2-hydroxypropyl] (Z)-docos-13-enoate

1.2 Other means of identification

Product number -
Other names 1,3-Dierucin

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:128389-74-2 SDS

128389-74-2Downstream Products

128389-74-2Relevant articles and documents

Enzymatic esterification of glycerol III. Lipase-catalyzed synthesis of regioisomerically pure 1,3-sn-diacylglycerols and 1(3)-rac-monoacylglycerols derived from unsaturated fatty acids

Waldinger,Schneider

, p. 1513 - 1519 (2007/10/03)

Lipases that display high regioselectivities and broad substrate tolerance were used as catalysts for the efficient esterification of glycerol under the conditions of irreversible acyl transfer. A variety of unsaturated fatty acids, such as oleic, linoleic, erucic, ricinolic, hydroxystearic and coriolic acid, were used for this purpose in the form of their vinyl esters. Suitable biocatalysts were chosen on the basis of systematic screening experiments regarding their regioselectivities (RE) and substrate tolerances. Distinct differences were found and expressed in numerical RE values as a measure for differences of these biocatalysts as being specific, selective, and nonspecific. Based on these experiments, a variety of molecules were synthesized on a preparative scale (>150 mmol) in good yield (ca. 85%) and with high regioisomerical purities (>95% RE).

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