22418-66-2

Usage

Uses

Used in Fragrance Industry:
3,7-DIMETHYL-2-METHYLENE-OCT-6-ENAL is used as a fragrance ingredient for its ability to add a strong, fruity scent to perfumes and other scented products. Its capacity to enhance the aroma of other compounds makes it a sought-after component in the creation of various fragrances.
Used in Flavor Industry:
In the flavor industry, 3,7-DIMETHYL-2-METHYLENE-OCT-6-ENAL is used as a flavoring agent to impart a fruity taste and aroma to food products. Its natural occurrence in fruits and vegetables contributes to its authenticity and appeal in enhancing the flavor profiles of various food items.
Used in Cosmetics Industry:
3,7-DIMETHYL-2-METHYLENE-OCT-6-ENAL is used as a scent component in cosmetics such as soaps, lotions, and other personal care products. Its strong, fruity odor adds a pleasant fragrance to these products, enhancing the sensory experience for the user.
Used in Essential Oils:
3,7-DIMETHYL-2-METHYLENE-OCT-6-ENAL is also used in the production of essential oils, where it contributes to the overall aroma and therapeutic properties of the oil. Its natural presence in various plant sources makes it a valuable addition to essential oil blends for aromatherapy and other applications.

InChI:InChI=1/C11H18O/c1-9(2)6-5-7-10(3)11(4)8-12/h6,8,10H,4-5,7H2,1-3H3

Upstream product

• 50-00-0 formaldehyd 
• 106-23-0 3,7-dimethyl-oct-6-enal 
• 18478-46-1 2-methylenecitronellol 

Downstream Products

• 1030630-94-4 4-[3-(3,3-dimethyloxiran-2-yl)-1-methylpropyl]-1-methylcyclohex-2-en-1-ol 
• 1723-81-5 1-methyl-4-(6-methylhept-5-en-2-yl)cyclohex-2-en-1-ol 
• 1723-80-4 4-(6-methyl-5-hepten-2-yl)-2-cyclohexen-1-one 

Relevant academic research and scientific papers

COMPOSITIONS COMPRISING ODORANTS

The present invention relates to odorous 2- and/or 3-substituted 3-(allyloxy)propenes which are useful as fragrance or flavor ingredients in particular in providing green, fruity, pear and/or waxy olfactory notes. The present invention also relates to novel perfume, aroma or deodorizing/masking compositions comprising said odorants.

1-HYDROXYMETHYL-1,2,2,6-TETRAMETHYL-CYCLOHEXANE AND DERIVATIVES THEREOF AND THEIR USE AS AROMA CHEMICALS

The invention relates to compounds of formula (A) as defined herein, and esters of the compound of formula (A), and ketones of the compound of formula (A). The invention further relates to a method for preparing compounds of formula (A) and esters of the compound of formula (A), and ketones of the compound of formula (A). The invention further relates to the use of at least one compound selected from compounds of formula (A) and the esters of a compound of formula (A) and the ketones of a compound of formula (A) as aroma chemical.

2,3,7-TRIMETHYLOCT-6-ENYL ACETATE AND 3,7-DIMETHYL-2-METHYLENE-OCT-6-ENYL ACETATE AND DERIVATIVES THEREOF AND THEIR USE AS AROMA CHEMICALS

The present invention relates to 2,3,7-Trimethyloct-6-enyl acetate and 3,7-dimethyl-2-methylene-oct-6-enyl acetate and derivatives thereof and their use as aroma chemicals.

MURGANTIOL AS A STINK BUG SYNERGISTIC ATTRACTANT FOR USE OUTDOORS

Provided herein are uses of the Harlequin bug pheromone, murgantiol, alone or in a synergistic combination with at least one other stink bug attractant, such as methyl (2E,4E,6Z)-decatrienoate or methyl (2E,4Z)-decadienoate, or both, for attracting stink bugs such as the brown marmorated stink bug in outdoor settings. Stink bug traps comprising murgantiol, or synergistic compositions comprising murgantiol with at least one other stink bug attractant, and methods of using these compositions in traps outdoors are provided. Compositions comprising murgantiol are also described as synergistic combinations of murgantiol with at least one other stink bug attractant.

Readily accessible oxazolidine nitroxyl radicals: Bifunctional cocatalysts for simplified copper based aerobic oxidation

Using a two-step procedure a range of bifunctional oxazolidine nitroxyl radicals have been prepared. The application of these co-catalysts to the copper-based aerobic oxidation of alcohols was then investigated. From these studies it was found that the parent tetramethyloxazolidine nitroxyl radical L1 was competent for oxidation in the presence of 2,2′-bipyridine, and the bifunctional pyridyl-containing nitroxyl radicals L2 and L3 could be used in the absence of additional coordinating ligands. Following optimization, the scope of this simplified transformation was explored, demonstrating that a range of primary and secondary benzylic alcohols are readily oxidized. In addition, the oxidation of allylic alcohols and hydroquinone can be achieved. Copyright

Highly stereoselective peptide modifications through Pd-catalyzed allylic alkylations of chelated peptide enolates

Deprotonation of peptides in the presence of zinc chloride gives rise to highly reactive nucleophiles that can be subjected to palladium-catalyzed allylic alkylation reactions. Excellent diastereoselectivities are obtained that are nearly independent of the allylic substrate used. By using this protocol, highly functionalized side chains can also be incorporated in excellent yields and selectivities. The stereochemicaloutcome of the reaction is exclusively controlled by the peptide chain as long as terminal π-allyl-palladium complexes are involved. Probably, there is a threefold coordination, at least, ofthe deprotonated peptide chain to the chelating zinc ion. In such metal peptide complexes, one face of the generated enolate is shielded by the side chain of the adjacent amino acid, thus directing the electrophilic attack onto the opposite face. This behavior explains why an S amino acid always generates an R amino acid (and the other way round).