29840-04-8

Basic information

• Product Name: allyl-(2-bromo-cyclohexyl)-ether
• Synonyms: allyl-(2-bromo-cyclohexyl)-ether
• CAS NO: 29840-04-8
• Molecular Weight: 219.121
• Mol File: 29840-04-8.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: allyl-(2-bromo-cyclohexyl)-ether(CAS DataBase Reference)
• NIST Chemistry Reference: allyl-(2-bromo-cyclohexyl)-ether(29840-04-8)
• EPA Substance Registry System: allyl-(2-bromo-cyclohexyl)-ether(29840-04-8)

Safety Data

• Hazardous Substances Data: 29840-04-8(Hazardous Substances Data)

Upstream product

• 107-18-6 allyl alcohol 
• 110-83-8 cyclohexene 
• 286-20-4 cyclohexane-1,2-epoxide 
• 81189-45-9 2-(prop-2-enyloxy)cyclohexan-1-ol 
• 560-95-2 bromotrinitromethane 

Downstream Products

• 16822-06-3 cis-3-methylenehexahydrobenzofuran-2-one 
• 51122-95-3 allyl Δ²-cyclohexenyl ether 
• 14289-64-6 allyl cyclohexyl ether 
• 370569-19-0 2-allyloxy-1-iodocyclohexane 

Relevant articles and documents

A New Synthetic Route to Alkenyl-substituted Tetrahydrofurans via Successive Intra- and Inter-molecular Radical Reactions

Tetrahydrofurans with alkenyl substituents were obtained by the radical cyclization of β-bromoethers using allyltri-n-butylstannane in a one-pot reaction.

Stereoselective cyclisation of the 2-allyloxytetrahydropyran-3-yl radical and related species: The influence of anomeric effects

Ring closures of the 2-allyloxytetrahydropyran-3-yl radical 1b, its mono-oxa analog 1d and the all carbon system 1a give mainly the cis-fused syn-substituted bicyclononylcarbinyl radicals 2b, 2d and 2a, but the mono- oxa radical 1c gives mainly the cis-fused anti-substituted radical 3c. Molecular mechanics calculations show that the unexpected failure of the dioxa radical lb to reflect the influence of the anomeric effect on the stereochemistry of cyclisation arises from the loss of one stabilising anomeric interaction in the conversion of the conformer 17 into either of the transition structures 16 or 19.