111171-96-1

Basic information

• Product Name: but-2-ene-1,1-diyldibenzene
• Synonyms: but-2-ene-1,1-diyldibenzene
• CAS NO: 111171-96-1
• Molecular Weight: 208.303
• Mol File: 111171-96-1.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: but-2-ene-1,1-diyldibenzene(CAS DataBase Reference)
• NIST Chemistry Reference: but-2-ene-1,1-diyldibenzene(111171-96-1)
• EPA Substance Registry System: but-2-ene-1,1-diyldibenzene(111171-96-1)

Safety Data

• Hazardous Substances Data: 111171-96-1(Hazardous Substances Data)

Upstream product

• 91-01-0 1,1-Diphenylmethanol 
• 1422177-77-2 2-(1,1-diphenylbut-3-en-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 91861-61-9 (1-Methyl-3,3-diphenyl-allyl)-triphenyl-phosphonium; iodide 
• 63537-05-3 (E)-(3-chlorobut-1-en-1-yl)benzene 
• 4286-85-5 4,4-diphenyl-1-butene 
• 998-30-1 Triethoxysilane 
• 187737-37-7 propene 
• 74-85-1 ethene 
• 908093-98-1 diazodiphenylmethane 
• 100-58-3 phenylmagnesium bromide 
• 56800-08-9 1,3-dichloro-1-butene 

Relevant articles and documents

Cationic and neutral diphenyldiazomethanerhodium(I) complexes as catalytically active species in the C-C coupling reaction of olefins and diphenyldiazomethane

Cationic rhodium(I) complexes cis-[Rh(acetone)2(L)(L')]+ (2: L=L'=C8H14; 3: L=C8H14; L'=PiPr3; 4: L= L'=PiPr3), prepared from [{RhCl-(C8H14)

Tandem reactions involving 1-silyl-3-boryl-2-alkenes. New access to (Z)-1-fluoro-1-alkenes, allyl fluorides, and diversely α-substituted allylboronates

The reactions of 1-silyl-3-boryl-2-alkenes with various electrophilic reagents (Selectfluor, N-halosuccinimides, benzhydryl, and propargylic alcohols in the presence of a Lewis acid, N-alkoxycarbonyliminium ion) have been investigated as new routes to α-substituted allylboronates. Further functional transformations, including allylboration, Suzuki coupling, protodeboronation, and cycloisomerization, have been carried out to illustrate the synthetic potential of these γ-borylallylsilanes.

Palladium catalyzed isomerization of alkenes: A pronounced influence of an o-phenol hydroxyl group

A novel palladium catalyzed isomerization of alkenes has been found, where an ortho-phenol hydroxyl group has a pronounced influence on the isomerization.