1178546-41-2

Basic information

• Product Name: (1-tert-butylcyclohexa-2,5-dien-1-yl)benzene
• Synonyms: (1-tert-butylcyclohexa-2,5-dien-1-yl)benzene
• CAS NO: 1178546-41-2
• Molecular Weight: 212.335
• Mol File: 1178546-41-2.mol

Chemical Properties

• CAS DataBase Reference: (1-tert-butylcyclohexa-2,5-dien-1-yl)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: (1-tert-butylcyclohexa-2,5-dien-1-yl)benzene(1178546-41-2)
• EPA Substance Registry System: (1-tert-butylcyclohexa-2,5-dien-1-yl)benzene(1178546-41-2)

Safety Data

• Hazardous Substances Data: 1178546-41-2(Hazardous Substances Data)

Upstream product

• 507-19-7 t-butyl bromide 
• 4794-05-2 3-phenyl-1,4-cyclohexadiene 
• 92-52-4 biphenyl 

Downstream Products

• 612-00-0 1,1'-ethylidenebis-benzene 
• 57123-34-9 1,1-diphenyl-3,3-dimethylbutane 
• 23586-64-3 (3,3-dimethylbut-1-ene-1,1-diyl)dibenzene 
• 395-24-4 4,4'-(ethane-1,1-diyl)bis(1-fluorobenzene) 
• 530-45-0 1,1-di(4-methylphenyl)ethane 

Relevant articles and documents

3-tert-Butyl-Substituted Cyclohexa-1,4-dienes as Isobutane Equivalents in the B(C6F5)3-Catalyzed Transfer Hydro-tert-Butylation of Alkenes

Cyclohexa-1,4-dienes with a tert-butyl group at C3 are shown to function as isobutane equivalents when activated by the strong boron Lewis acid tris(pentafluorophenyl)borane. The hitherto unprecedented transfer hydro-tert-butylation from one unsaturated hydrocarbon to another is achieved with 1,1-diarylalkenes as substrates, thereby presenting itself as a new way of incorporating tertiary alkyl groups into carbon frameworks. Transient carbocation intermediates give rise to competing reaction pathways that could not be fully suppressed.

Birch reductive alkylation of biaryls: Scope and limitations

(Chemical Equation Presented) Birch reductive alkylation of biaryls has been carried out by varying the nature of the substituents on the aromatic rings. Our investigations have focused on electron-rich substituents such as OMe, OH, and NR2 gro