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22425-82-7 Usage

General Description

Methyl maslinate is a chemical compound belonging to the class of organic compounds known as flavonoids. It is found naturally in a variety of plants and fruits, including apples, strawberries, and grapes. Methyl maslinate has been studied for its potential therapeutic properties, including antioxidant, anti-inflammatory, and anti-cancer effects. It has also been investigated for its potential role in promoting cardiovascular health and preventing age-related diseases. The compound is of interest to researchers due to its diverse biological activities and potential health benefits, but further studies are needed to fully understand its mechanisms of action and potential applications in medicine and nutrition.

Check Digit Verification of cas no

The CAS Registry Mumber 22425-82-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,4,2 and 5 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 22425-82:
87 % 10 = 7
So 22425-82-7 is a valid CAS Registry Number.



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


1.1 GHS Product identifier

Product name methyl (4aS,6aR,6aS,6bR,10R,11R,12aR,14bR)-10,11-dihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate

1.2 Other means of identification

Product number -
Other names Crategolic acid methyl ester

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:22425-82-7 SDS

22425-82-7Relevant articles and documents

Different pathways for the deoxygenation of the A-ring of natural triterpene compounds

Parra, Andres,Lopez, Pilar E.,Garcia-Granados, Andres

scheme or table, p. 177 - 196 (2010/05/18)

Some deoxygenation pathways were tested to remove the hydroxyl groups of the natural triterpenes oleanolic acid and maslinic acid to obtain a practical starting material for the semisynthesis of other interesting organic synthons. Different deoxygenation processes were carried out starting from these triterpenic acids or from several derivatives such as methyl esters and epoxy derivatives. The hydroxyl groups were transformed into some intermediate compounds including xanthyl, thiocarbonyl or tosyl derivatives. The opening of the oxirane ring between C-2 and C-3 was also achieved through different methods using deoxygenating reagents such as Me3SiCl/NaI, WCl 4/n-BuLi and Cp2TiCl.

Further triterpenes from Melissa officinalis L


, p. 603 - 612 (2007/10/11)


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