5041-39-4

Basic information

• Product Name: Benzene, 1,1'-[(1E)-1-butyl-1,2-ethenediyl]bis-
• CAS NO: 5041-39-4
• Molecular Formula: C18H20
• Molecular Weight: 236.357
• Mol File: 5041-39-4.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: Benzene, 1,1'-[(1E)-1-butyl-1,2-ethenediyl]bis-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1,1'-[(1E)-1-butyl-1,2-ethenediyl]bis-(5041-39-4)
• EPA Substance Registry System: Benzene, 1,1'-[(1E)-1-butyl-1,2-ethenediyl]bis-(5041-39-4)

Safety Data

• Hazardous Substances Data: 5041-39-4(Hazardous Substances Data)

Upstream product

• 100347-31-7 C₁₆H₃₆Ce^(1-)*Li⁽¹⁺⁾ 
• 1689-71-0 cis-1,2-diphenyloxirane 
• 1439-07-2 trans-Stilbene oxide 
• 16897-96-4 (Z)-2,3-diphenylhept-2-enoic acid 
• 109-72-8 n-butyllithium 
• 301298-30-6 1-tert-Butyldiphenylsilyl-1-phenylhexan-2-one 
• 501-65-5 diphenyl acetylene 
• 591-50-4 iodobenzene 
• 1129-65-3 (hex-1-yn-1-yl)benzene 
• 1009-14-9 phenyl butyl ketone 
• 140-29-4 phenylacetonitrile 
• 143-66-8 sodium tetraphenyl borate 
• 100-58-3 phenylmagnesium bromide 
• 693-02-7 hex-1-yne 

Relevant articles and documents

Iterative synthesis of alkenes by insertion of lithiated epoxides into boronic esters

The insertion of lithiated epoxides into boronic esters followed by thermal syn-elimination provides a stereospecific entry to alkenes. This process avoids transition metals and is amenable to iteration to provide higher substitution patterns.

Ambient arylmagnesiation of alkynes catalysed by ligandless nickel(ii)

A simple and efficient catalytic arylmagnesiation of diarylacetylenes and aryl(alkyl)acetylenes is accomplished by NiCl2·6H2O at r.t. in the absence of stabilising ligands. The corresponding tetra-substituted alkenes can be obtained in good yields by subsequent treatment with different electrophiles. The Royal Society of Chemistry 2013.

Palladium-catalyzed hydrophenylation of alkynes with sodium tetraphenylborate under mild conditions

(Chemical Equation Presented) In an aqueous solution of acetic acid, PdCl2(PPh3)2 showed high catalytic activity for the hydrophenylation of both terminal and internal alkynes with sodium tetraphenylborate (NaBPh4) under mild conditions, affording phenyl alkenes in moderate to excellent yields.