27905-65-3

Basic information

• Product Name: 2,6-DIPHENYL-1,6-HEPTADIENE
• Synonyms: (1-Methylene-5-phenyl-5-hexenyl)benzene;2,6-Diphenyl-1,7-heptadiene;2,6-DIPHENYL-1,6-HEPTADIENE
• CAS NO: 27905-65-3
• Molecular Formula: C₁₉H₂₀
• Molecular Weight: 248.36
• Mol File: 27905-65-3.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 390.5°Cat760mmHg
• Flash Point: 208.1°C
• Appearance: /
• Density: 0.96g/cm³
• CAS DataBase Reference: 2,6-DIPHENYL-1,6-HEPTADIENE(CAS DataBase Reference)
• NIST Chemistry Reference: 2,6-DIPHENYL-1,6-HEPTADIENE(27905-65-3)
• EPA Substance Registry System: 2,6-DIPHENYL-1,6-HEPTADIENE(27905-65-3)

Safety Data

• Hazardous Substances Data: 27905-65-3(Hazardous Substances Data)

Usage

General Description

2,6-DIPHENYL-1,6-HEPTADIENE is a compound belonging to the class of organic chemicals known as polyene hydrocarbons. It is a colorless liquid that is insoluble in water but soluble in organic solvents. 2,6-DIPHENYL-1,6-HEPTADIENE has potential biological activity and is used in the synthesis of other organic compounds. It is also known for its ability to undergo various chemical reactions, making it valuable in organic chemistry research and manufacturing processes. Additionally, 2,6-DIPHENYL-1,6-HEPTADIENE is used as a component in the production of fragrances and flavorings.

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 articles and documents

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.

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