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7439-44-3

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7439-44-3 Usage

General Description

Methyl brassidate is a natural compound found in various plants, including cabbage and mustard. It is a member of the class of organic compounds known as fatty acid methyl esters and is derived from the fatty acid, erucic acid. Methyl brassidate has been studied for its potential as a biofuel due to its high energy content and low freezing point. Additionally, it has shown potential as a bioactive compound, with anti-inflammatory and anti-cancer properties. Its specific chemical structure and functional properties make it a versatile compound with potential applications in the food, pharmaceutical, and energy industries.

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 articles and documents

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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