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43126-29-0

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43126-29-0 Usage

Description

(E)-megastigma-4,8-diene-3,7-dione is a diketone chemical compound that plays a significant role in the formation of aroma and flavor in various organisms, such as plants and fungi. It is characterized by its potent odor and strong, sweet, and floral scent, making it a valuable component in the production of perfumes, flavorings, and fragrances. Furthermore, research has indicated potential medicinal properties, including anti-inflammatory and anti-cancer effects.

Uses

Used in Perfumery and Fragrance Industry:
(E)-megastigma-4,8-diene-3,7-dione is used as a key component in the creation of perfumes and fragrances due to its potent odor and strong, sweet, and floral scent. It contributes to the overall aroma and appeal of these products, enhancing their sensory experience for consumers.
Used in Flavorings Industry:
In the production of flavorings, (E)-megastigma-4,8-diene-3,7-dione is utilized as a flavoring agent, particularly for creating floral and fruity flavors. Its unique scent profile adds depth and complexity to various food and beverage products, enhancing their taste and overall enjoyment.
Used in Pharmaceutical Research:
(E)-megastigma-4,8-diene-3,7-dione is also used in pharmaceutical research due to its potential medicinal properties. Some studies have suggested that it may have anti-inflammatory and anti-cancer effects, making it a promising candidate for further investigation and potential development into therapeutic applications.
Used in Essential Oils:
(E)-megastigma-4,8-diene-3,7-dione is commonly found in essential oils, where it contributes to the overall scent and therapeutic properties of these oils. Essential oils containing (E)-megastigma-4,8-diene-3,7-dione are often used in aromatherapy and other holistic health practices for their potential benefits to the mind and body.

Check Digit Verification of cas no

The CAS Registry Mumber 43126-29-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,3,1,2 and 6 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 43126-29:
(7*4)+(6*3)+(5*1)+(4*2)+(3*6)+(2*2)+(1*9)=90
90 % 10 = 0
So 43126-29-0 is a valid CAS Registry Number.

43126-29-0Downstream Products

43126-29-0Relevant articles and documents

Selective oxygenation of ionones and damascones by fungal peroxygenases

Aranda, Carmen,Babot, Esteban D.,Del R?o, José C.,Gutiérrez, Ana,Hofrichter, Martin,Kiebist, Jan,Mart?nez, Angel T.,Scheibner, Katrin,Ullrich, René

, p. 5375 - 5383 (2020/06/08)

Apocarotenoids are among the most highly valued fragrance constituents, being also appreciated as synthetic building blocks. This work shows the ability of unspecific peroxygenases (UPOs, EC1.11.2.1) from several fungi, some of them being described recently, to catalyze the oxyfunctionalization of α- and β-ionones and α- and β-damascones. Enzymatic reactions yielded oxygenated products such as hydroxy, oxo, carboxy, and epoxy derivatives that are interesting compounds for the flavor and fragrance and pharmaceutical industries. Although variable regioselectivity was observed depending on the substrate and enzyme, oxygenation was preferentially produced at the allylic position in the ring, being especially evident in the reaction with α-ionone, forming 3-hydroxy-α-ionone and/or 3-oxo-α-ionone. Noteworthy were the reactions with damascones, in the course of which some UPOs oxygenated the terminal position of the side chain, forming oxygenated derivatives (i.e., the corresponding alcohol, aldehyde, and carboxylic acid) at C-10, which were predominant in the Agrocybe aegerita UPO reactions, and first reported here.

Butenoyl-cyclohexanones

-

, (2008/06/13)

Use of oxygenated alicyclic compounds, some of which are new, as perfuming and/or flavouring ingredients in the manufacture of perfumes and perfumed products and/or in the preparation of artificial flavours for foodstuffs, animal feeds, beverages, pharmac

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