62238-28-2

Usage

Uses

Used in Fragrance Industry:
2,5,5-Trimethyl-1,6-heptadiene is used as a fragrance ingredient for its pleasant scent, which is similar to that of hops and cannabis. It contributes to the overall aroma of various perfumes and other scented products.
Used in Flavoring Industry:
In the flavoring industry, 2,5,5-Trimethyl-1,6-heptadiene is used as a flavoring agent to impart a unique taste and aroma to food and beverage products, particularly those that require a hop-like or cannabis-like flavor profile.
Used in Brewing Industry:
2,5,5-Trimethyl-1,6-heptadiene is used as a key component in the brewing of beer, where it contributes to the characteristic aroma and flavor of certain hop varieties. Its presence enhances the overall taste and sensory experience of the beer.
Used in Medicinal Applications:
In the field of medicine, 2,5,5-Trimethyl-1,6-heptadiene is studied for its potential medicinal properties, such as anti-inflammatory, analgesic, and sedative effects. It may be used in the development of pharmaceutical products or as a complementary therapy for various conditions.

Upstream product

• 35189-96-9 3-methyl-2-butenylmagnesium chloride 
• 78-79-5 isoprene 
• 76588-94-8 2,5,6-trimethyl-1,5-heptadiene 

Relevant academic research and scientific papers

Photochemistry of Alkenes. 6. Direct Irradiation of 1,5-Hexadienes: and Sigmatropic Allyl Shifts

The photochemical behavior of a series of alkyl-substituted 1,5-hexadienes has been studied.Competing allylcyclopropane formation and rearrangement to an isomeric 1,5-hexadiene via competing and sigmatropic allyl shifts, respectively, were observed.In one case a product (30 from 27) and in another a product (35 from 31) was obtained, but only in low yield.Extensive cis trans isomerization competed with the allyl shifts, and, in addition, other products were obtained which are characteristic of the photochemical behavior of isolated double bonds.At low conversion diene 10t underwent stereoselective rearrangement to 8t and 11t, whereas the cis isomer 10c afforded mixtures of the cis and trans isomers of 8 and 11.Attempts to induce the allyl migrations by sensitization with p-xylene or by irradiation at 254 nm afforded only cis trans isomerization.It is concluded that the allyl migrations occur via an excited state involving interaction between the double bonds and requiring a conformation in which the central C3-C4 bond is in a plane orthogonal to both double bonds, as proposed previously.In contrast with the acyclic dienes, 1,5-cyclooctadiene (50) afforded products 51-53 from competing , , and allyl shifts, respectively.The divergent behavior in this case apparently arises because appropriate interaction between the two double bonds can occur only in the boat conformation.