104729-88-6

Basic information

• Product Name: (E)-1-(4-(tert-butyl)phenyl)-1,2-diphenylethylene
• Synonyms: (E)-1-(4-(tert-butyl)phenyl)-1,2-diphenylethylene
• CAS NO: 104729-88-6
• Molecular Weight: 312.455
• Mol File: 104729-88-6.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (E)-1-(4-(tert-butyl)phenyl)-1,2-diphenylethylene(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-1-(4-(tert-butyl)phenyl)-1,2-diphenylethylene(104729-88-6)
• EPA Substance Registry System: (E)-1-(4-(tert-butyl)phenyl)-1,2-diphenylethylene(104729-88-6)

Safety Data

• Hazardous Substances Data: 104729-88-6(Hazardous Substances Data)

Upstream product

• 121149-70-0 1-[4-(1,1-dimethylethyl)phenyl]-2-phenylethanone 
• 253185-03-4 tert-butylbenzene 
• 103-80-0 phenylacetyl chloride 
• 1255083-15-8 (4-(tert-butyl) phenyl)(phenyl)methanethione 
• 908094-04-2 phenyldiazomethane 
• 1666-17-7 benzaldehyde p-toluenesulfonylhydrazone 
• 14447-41-7 (E)-1-bromo-1,2-diphenylethene 
• 123324-71-0 p-tert-butylphenylboronic acid 
• 22679-54-5 4-tert-butylbenzophenone 
• 13440-24-9 1,2-dibromo-1,2-diphenylethane 
• 3972-65-4 1-bromo-4-tert-butylbenzene 
• 221006-75-3 1-phenyl-2-phenylethyleneboronic acid pinacol ester 
• 501-65-5 diphenyl acetylene 
• 7498-54-6 3-t-Butylbenzoic acid 

Relevant articles and documents

Elucidation of the stereochemistry of thiirane formation from a 1λ4,2-dithietane bearing two chiral carbon centers

A tetracoordinated sulfurane bearing a 1λ4,2-dithietane moiety, whose 3- and 4-positions were chiral carbon centers, was synthesized. Its thermolysis gave the corresponding thiirane as a single diastereomer, whose configuration and stereochemis

Palladium-catalyzed desulfitative hydroarylation of alkynes with sodium sulfinates

A palladium-catalyzed desulfitative hydroarylation of alkynes with aryl sulfinic acid sodium salts is described. The reaction showed good regio- and stereoselectivity, and afforded the hydroarylation products in good yields. Various functional groups were well tolerated under the optimized reaction conditions.