60014-85-9

Basic information

• Product Name: Cyclohexane, (dibromomethylene)-
• CAS NO: 60014-85-9
• Molecular Formula: C7H10Br2
• Molecular Weight: 253.964
• Mol File: 60014-85-9.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: Cyclohexane, (dibromomethylene)-(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclohexane, (dibromomethylene)-(60014-85-9)
• EPA Substance Registry System: Cyclohexane, (dibromomethylene)-(60014-85-9)

Safety Data

• Hazardous Substances Data: 60014-85-9(Hazardous Substances Data)

Upstream product

• 108-94-1 cyclohexanone 
• 52183-68-3 1-dibromomethyl-1-cyclohexanol 
• 558-13-4 carbon tetrabromide 
• 6156-08-7 cyclohexanone hydrazone 
• 60014-80-4 1-dibromomethyl-1-(trimethylsiloxy)cyclohexane 

Downstream Products

• 69190-57-4 <1,1-bis(phenylthio)methylene>cyclohexane 
• 89438-16-4 <1,1-bis(phenylseleno)methylene>cyclohexane 
• 1121-49-9 bromomethylenecyclohexane 
• 87372-65-4 (bromomethoxymethylene)cyclohexane 
• 67091-34-3 (diiodomethylene)cyclohexane 
• 90598-25-7 1-Brom-1-cyclohexyliden-2-butanol 
• 59643-60-6 (3,3-Dimethyl-1-butenyliden)cyclohexan 
• 59643-63-9 (2-cyclohexylidene ethenyl)-benzene 
• 90598-33-7 (2-Brom-2-cyclohexyliden-1-ethenylethyl)-(trimethylsilyl)-ether 
• 90598-31-5 (2-Brom-2-cyclohexyliden-1-ethylethyl)-(trimethylsilyl)-ether 
• 90598-34-8 (2-Brom-2-cyclohexyliden-1-phenylethyl)-(trimethylsilyl)-ether 
• 90598-35-9 <2-Brom-2-cyclohexyliden-1-(4-methoxyphenyl)ethyl>-(trimethylsilyl)-ether 
• 90598-36-0 <2-(4-Methoxyphenyl)ethenyliden>cyclohexan 
• 2719-26-8 N-phenylcyclohexanamide 

Relevant articles and documents

Long-distance electronic coupling in diferrocenyl compounds with cross-conjugated germinal-diethynylethene bridges

A series of germinal-diethynylethene (gem-DEE) bridged diferrocenyl compounds, including 1,1-[bis(ferrocenylethynyl)methylene]cyclohexane (1), 1,1-[bis(ferrocenylethynyl)methylene]tetrahydro-2H-pyran (2), and 1,1-[bis(ferrocenylethynyl)methylene]tetrahydr

Palladium(0)-catalyzed cross-coupling of 1,1-diboronates with vinyl bromides and 1,1-dibromoalkenes

Palladium-catalyzed cross-coupling reactions of 1,1-diboronates with vinyl bromides and dibromoalkenes were found to afford 1,4-dienes and allenes, respectively. These reactions utilize the high reactivities of both 1,1-diboronates and allylboron intermediates generated in the initial coupling.

Ruthenium-catalyzed cycloisomerization of cis-3-en-1-ynes to cyclopentadiene and related derivatives through a 1,5-sigmatropic hydrogen shift of ruthenium vinylidene intermediates

We report a new ruthenium-catalyzed cycloisomerization of unactivated cis-3-en-1-ynes, which produces substituted cyclopentadiene and related derivatives. The mechanism of this cyclization is proposed to involve a [1,5]-sigmatropic hydrogen shift of ruthenium-vinylidene intermediates on the basis of deuterium-labeling experiments. Copyright