38328-19-7

Basic information

• Product Name: hexa-1,5-diene-1,1-diyldibenzene
• Synonyms: hexa-1,5-diene-1,1-diyldibenzene
• CAS NO: 38328-19-7
• Molecular Weight: 234.341
• Mol File: 38328-19-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: hexa-1,5-diene-1,1-diyldibenzene(CAS DataBase Reference)
• NIST Chemistry Reference: hexa-1,5-diene-1,1-diyldibenzene(38328-19-7)
• EPA Substance Registry System: hexa-1,5-diene-1,1-diyldibenzene(38328-19-7)

Safety Data

• Hazardous Substances Data: 38328-19-7(Hazardous Substances Data)

Upstream product

• 26189-62-8 phenyl 2,2-diphenylethenyl sulfone 
• 7051-34-5 cyclopropylcarbinyl bromide 
• 3923-51-1 1,1-diphenylprop-2-en-1-ol 
• 72824-04-5 2-Allyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 119-61-9 benzophenone 
• 556-56-9 allyl iodid 
• 4801-15-4 3-bromo-1,1-diphenyl-1-propene 
• 1730-25-2 allylmagnesium bromide 

Downstream Products

• 119-61-9 benzophenone 
• 2100-17-6 4-pentenal 
• 207455-92-3 1,1-diphenylhex-5-en-2-ol 
• 7714-72-9 6,6-diphenylfulvene 
• 1351520-88-1 6-deuterio-1,1-diphenyl-1-hexene 

Relevant articles and documents

Alkenylation of unactivated alkyl bromides through visible light photocatalysis

Two visible-light driven alkenylation reactions of unactivated alkyl bromides, which were enabled by the use of Ir(dF(CF3)ppy)2(dtbbpy)PF6 as the photocatalyst and (TMS)3SiH as the atom transfer reagent to activate the alkyl bromides, were described for the first time. These protocols can be used to produce a variety of alkenes from easily available feedstock with good reaction efficiency and high chemoselectivity under mild reaction conditions. To further demonstrate the applicability of the present strategy, the alkenylation of bioactive molecules and glycosyl bromides, as well as the alkynylation of unactivated alkyl bromides, was proven to be feasible.

Selective Alkylation and Allylation of Allylic Halides by Tetraorganoidates: Regio- and Stereo-selective Synthesis of Rosefuran and Sesquirosefuran

Tetraalkylindanes regioselectively alkylate allylic bromides at the α-carbon.In this way, 1,5-dienes have been regio- and stereo-selectively synthesized by the allyl-allyl coupling of allylic bromides and allylic indates, including rosefuran 1 and sequirosefuran 3.