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37910-77-3

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37910-77-3 Usage

Uses

Erucic Acid Ethyl Ester is the ethyl ester of Erucic acid (E649900) which is a long-chain alcohol that acts as an inhibitor of fatty acid oxidation in the heart. Erucic acid originates in rapeseed plants, and is the major fatty acid constituent of rapeseed plant oil extracts and canola oil.

Definition

ChEBI: A long-chain fatty acid ethyl ester resulting from the formal condensation of the carboxy group of (13Z)-docosenoic acid with the hydroxy group of ethanol.

Check Digit Verification of cas no

The CAS Registry Mumber 37910-77-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,9,1 and 0 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 37910-77:
(7*3)+(6*7)+(5*9)+(4*1)+(3*0)+(2*7)+(1*7)=133
133 % 10 = 3
So 37910-77-3 is a valid CAS Registry Number.
InChI:InChI=1/C24H46O2/c1-3-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-24(25)26-4-2/h11-12H,3-10,13-23H2,1-2H3/b12-11-

37910-77-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl (13Z)-docosenoate

1.2 Other means of identification

Product number -
Other names Eruaeure-aethylester

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:37910-77-3 SDS

37910-77-3Relevant articles and documents

Preparation method of nervonic acid and nervonic acid

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Paragraph 0049-0051; 0056, (2020/07/27)

The invention discloses a preparation method of nervonic acid and nervonic acid. The preparation method comprises the following steps: preparing a Grignard reagent from 1-bromo-cis-13-docosaene, and carrying out an epoxy ring-opening reaction on the Grignard reagent, cuprous iodide and ethylene oxide to synthesize 1-hydroxy-cis-15-tetracosaene; and preparing nervonic acid by carrying out oxidationreaction on 1-hydroxy-cis-15-tetracosaene, iodobenzene acetate and TEMPO. By means of chemical synthesis, erucic acid is used as a raw material, and synthesis of nervonic acid is completed through esterification, reduction, bromination, Grignard reaction and oxidation. The method for synthesizing nervonic acid has the advantages of cheap and accessible raw materials, high yield, high product purity and the like, and is easy to operate.

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