5009-92-7

Basic information

• Product Name: 1-methyl-1-butylcyclohexane
• Synonyms: 1-methyl-1-butylcyclohexane
• CAS NO: 5009-92-7
• Molecular Weight: 154.296
• Mol File: 5009-92-7.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1-methyl-1-butylcyclohexane(CAS DataBase Reference)
• NIST Chemistry Reference: 1-methyl-1-butylcyclohexane(5009-92-7)
• EPA Substance Registry System: 1-methyl-1-butylcyclohexane(5009-92-7)

Safety Data

• Hazardous Substances Data: 5009-92-7(Hazardous Substances Data)

Upstream product

• 693-03-8 n-butyl magnesium bromide 
• 931-78-2 1-chloro-1-methylcyclohexane 
• 108-94-1 cyclohexanone 
• 24406-16-4 lithium di-n-butylcuprate 
• 35324-50-6 p-Chlorphenyl-cyclohexylidenmethyl-sulfon 
• 13152-41-5 butylcycloheptanone 
• 5445-30-7 1-butyl-cyclohexanol 
• 544-97-8 dimethyl zinc(II) 
• 1119-90-0 di-n-butylzinc 
• 28320-90-3 1-n-Butyl-1-hydroxy-cyclohexan 
• 994-79-6 tetrabutylsilane 
• 40582-86-3 p-Chlorphenyl-(1-butylcyclohexyl)-methylsulfon 

Downstream Products

• 96-37-7 methyl-cyclopentane 
• 108-38-3 m-xylene 
• 91-20-3 naphthalene 
• 104-51-8 1-butylbenzene 
• 95-63-6 1,2,4-Trimethylbenzene 
• 82166-21-0 methyl cyclohexane 
• 108-88-3 toluene 

Relevant articles and documents

IONIC ALKYLATION OF TERTIARY ALKYL HALIDES WITH TETRAALKYLSILANES

In the reaction of tertiary alkyl halides with tetraethyl-, tetrapropyl-, tetrabutyl-, and tetraamylsilane in the presence of AlX3 the halogen atom is substituted by the alkyl group with the formation of the corresponding saturated hydrocarbons containing a quaternary carbon atom.As a result of the hydride mobility of the β-hydrogen atom in the tetraalkylsilane ionic hydrogenolysis of the substrate occurs in addition to alkylation, and the degree of hydrogenolysis depends on the alkyl substituent in the silane.

Geminale Dialkylierung von Ketonen mit Grignard-Verbindungen und Methyltitan(IV)-chloriden

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