26613-38-7

Basic information

• Product Name: Benzene, 1,1'-(1-ethyl-1-methyl-1,2-ethanediyl)bis-
• CAS NO: 26613-38-7
• Molecular Formula: C17H20
• Molecular Weight: 224.346
• Mol File: 26613-38-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzene, 1,1'-(1-ethyl-1-methyl-1,2-ethanediyl)bis-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1,1'-(1-ethyl-1-methyl-1,2-ethanediyl)bis-(26613-38-7)
• EPA Substance Registry System: Benzene, 1,1'-(1-ethyl-1-methyl-1,2-ethanediyl)bis-(26613-38-7)

Safety Data

• Hazardous Substances Data: 26613-38-7(Hazardous Substances Data)

Upstream product

• 13144-95-1 2-chloro-2-phenylbutane 
• 6921-34-2 benzylmagnesium chloride 
• 75-16-1 methylmagnesium bromide 
• 100-39-0 benzyl bromide 
• 93-55-0 1-phenyl-propan-1-one 
• 34235-81-9 3-methyl-2-(4-methylphenylsulfonamido)pentanoic acid 
• 71-43-2 benzene 
• 3968-69-2 (+/-)-2-methyl-2-phenyl-butyryl chloride 
• 51018-80-5 2-methyl-2-phenylbutanoic acid 
• 6948-04-5 1-methyl-1-phenyl-n-propylamine 
• 29555-79-1 (+/-)-N-Benzyl-1-methyl-1-phenylpropylamine 

Relevant articles and documents

Decarbonylative diarylation reaction of N-tosylated α-amino acids

The reaction of various N-tosylated α-amino acids with arenes in the presence of sulfuric acid afforded the corresponding diarylated derivatives in moderate yields, which were generated via decarbonylative arylation followed by Friedel-Crafts reaction of the generated tosylamide derivatives.

Vanadium(II) complexes as efficient reagents for direct construction of asymmetric quaternary carbons from carbonyl compounds

Direct geminal diallylation of propiophenone with allyl bromide has been achieved in the presence of vanadium(II) species. By applying this method, direct construction of asymmetric quaternary carbons from propiophenone has been accomplished. Strong oxophilicity of the low-valent vanadium facilitated the deoxygenative reaction. The present reaction is characteristic of vanadium complexes.