27905-65-3

Usage

Uses

Used in Organic Chemistry Research:
2,6-DIPHENYL-1,6-HEPTADIENE is used as a research compound for its ability to participate in a wide range of chemical reactions, making it a valuable asset in the field of organic chemistry.
Used in Synthesis of Organic Compounds:
2,6-DIPHENYL-1,6-HEPTADIENE serves as a key intermediate in the synthesis of other organic compounds, contributing to the development of new chemical entities.
Used in Fragrance and Flavoring Production:
2,6-DIPHENYL-1,6-HEPTADIENE is used as a component in the production of fragrances and flavorings, leveraging its chemical properties to create desired scents and tastes in various consumer products.
Used in Manufacturing Processes:
Its role in manufacturing processes is significant, as it is involved in the creation of a variety of products, highlighting its utility in industrial applications.

Upstream product

• 1779-49-3 Methyltriphenylphosphonium bromide 
• 94383-67-2 1,5-diphenylbicyclo<3.2.0>heptane 
• 6263-83-8 1,5-diphenyl-1,5-pentanedione 
• 19493-09-5 Methylenetriphenylphosphorane 
• 2873-74-7 gloutaric dichloride 
• 71-43-2 benzene 

Downstream Products

• 68305-42-0 6-methyl-1,5-diphenyl-6-phospha-bicyclo[3.2.1]octane 6exo-oxide 
• 68305-42-0 6-methyl-1,5-diphenyl-6-phospha-bicyclo[3.2.1]octane 6endo-oxide 
• 6263-83-8 1,5-diphenyl-1,5-pentanedione 
• 94383-67-2 1,5-diphenylbicyclo<3.2.0>heptane 
• 157367-60-7 1,5-Diphenyl-6,7-dioxa-bicyclo[3.2.2]nonane 
• 94383-67-2 1,5-Diphenylbicyclo<3.2.0>heptane 
• 94385-00-9 cis-1,4-Diphenyl-cycloheptandiol-(1,4) 

Relevant academic research and scientific papers

Tailoring flavins for visible light photocatalysis: organocatalytic [2+2] cycloadditions mediated by a flavin derivative and visible light

A new application of flavin derivatives in visible light photocatalysis was found. 1-Butyl-7,8-dimethoxy-3-methylalloxazine, when irradiated by visible light, was shown to allow an efficient cyclobutane ring formation via an intramolecular [2+2] cycloaddition of both styrene dienes, considered as electron-rich substrates, and electron-poor bis(arylenones), presumably proceeding via an energy transfer mechanism.

Photoinduced Electron Transfer (PET) cyclization and photooxygenation of 2,6-diaryl-1,6-heptadienes and 2,7-diaryl-1,7-octadienes

The 2,6-diaryl-substituted 1,6-heptadienes 3a-c and the 2,7-diaryl-substituted 1,7-octadienes 4a-b were cleanly converted into the corresponding anellated cyclobutanes 5 and 6, resp., when irradiated under photoelectron-transfer conditions (9,10-dicyanoanthracene in acetonitrile). Only for 4c did the rearranged compound 7c become the dominant photoproduct. Oxygen trapping experiments with formation of endoperoxides 8, 9 were successful in the case of the electron-rich substrates 3b, c and 4c. VCH Verlagsgesellschaft mbH, 1996.

Mechanism-based design of simple, symmetrical, easily prepared, potent antimalarial endoperoxides

Mechanism-based design, two-step synthesis, and in vitro antimalarial testing showed thermally stable, crystalline, bicyclic endoperoxides 2a and 2b to be potent antimalarials. Their reduction by FeBr2 proceeds via oxy-radicals and then carbon

A "frustrated" cope rearrangement: Thermal interconversion of 2,6-diphenylhepta-1,6-diene and 1,5-diphenylbicyclo[3.2.0]heptane

The title reaction constitutes a reliable model of a nonconcerted, diradical mechanism closely related to a Cope rearrangement. Its activation parameters relate to a transition state approximated by 1,5-diphenylcyclohepta-1,5-diyl (7). Force field calcula