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Methyl brassidate, a natural compound found in plants such as cabbage and mustard, belongs to the class of organic compounds known as fatty acid methyl esters. Derived from erucic acid, this versatile compound exhibits high energy content, low freezing point, and bioactive properties, including anti-inflammatory and anti-cancer effects. Its unique chemical structure and functional attributes position it for potential applications across the food, pharmaceutical, and energy industries.

7439-44-3

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7439-44-3 Usage

Uses

Used in Energy Industry:
Methyl brassidate is used as a potential biofuel for its high energy content and low freezing point, making it a promising candidate for sustainable and efficient energy production.
Used in Food Industry:
Methyl brassidate is used as a bioactive compound for its anti-inflammatory properties, contributing to the development of health-promoting food products.
Used in Pharmaceutical Industry:
Methyl brassidate is used as a potential anti-cancer agent, owing to its bioactive properties that can help in the development of novel therapeutic approaches to combat cancer.

Check Digit Verification of cas no

The CAS Registry Mumber 7439-44-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,3 and 9 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7439-44:
(6*7)+(5*4)+(4*3)+(3*9)+(2*4)+(1*4)=113
113 % 10 = 3
So 7439-44-3 is a valid CAS Registry Number.
InChI:InChI=1/C23H44O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23(24)25-2/h10-11H,3-9,12-22H2,1-2H3/b11-10+

7439-44-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl Brassidate

1.2 Other means of identification

Product number -
Other names Methyl trans-13-docosenoate

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:7439-44-3 SDS

7439-44-3Relevant academic research and scientific papers

Synthesis of Very Long Fatty Acid Methyl Esters

Kling, Marcel R.,Easton, Christopher J.,Poulos, Alf

, p. 1183 - 1190 (2007/10/02)

Phosphoranes, produced by treating alkyltriphenylphosphonium bromides with lithium hexamethyldisilazide, reacted with ω-oxo esters to give modest yields of the corresponding methyl cis-alkenoates.By an alternative method, treatment of ω-iodo esters with the complexes formed from reactions of alkylcopper(I) and Grignard reagents gave methyl alkanoates, cis-alkenoates, and methylene-interrupted cis,cis-alka-dienoates and cis,cis,cis-trienoates.The stereochemical integrity of the esters was determined by 13C NMR spectroscopy.

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