31683-73-5

Usage

Chemical structure

The compound has a bicyclic structure, which includes a bicyclo[2.2.1]heptane ring system.

Building block

It is commonly used as a building block in the synthesis of various pharmaceuticals and organic compounds.

Biological activities

The compound is known to exhibit diverse biological activities, making it a potential candidate for drug development.

Reactivity

Its unique structure and reactivity make it a valuable intermediate in organic chemistry.

Applications

It is widely used in the production of fragrances, flavors, and other fine chemicals.

Versatility

1-(bicyclo[2.2.1]hept-2-yl)propan-2-one is a versatile compound with potential applications in various industries.

Upstream product

• 65700-06-3 percarbonate de O,O-tert-butyle et O-isopropyle 
• 279-23-2 norbornane 
• 498-66-8 norborn-2-ene 
• 67-64-1 acetone 
• 498-66-8 norbornene 
• 80484-22-6 Norcampher-hydrazon 
• 58426-15-6 1-iodonorbornene 
• 46369-53-3 bis(acetylacetonato)copper(II) 
• 56561-19-4 1-Bicyclo[2.2.1]hept-(2E)-ylidene-propan-2-one 
• 279-23-2 norbornene 

Relevant academic research and scientific papers

Highly efficient methyl ketone synthesis by water-assisted C-C coupling between olefins and photoactivated acetone

(Chemical Equation Presented) Photoirradiation of an acetone/water mixture containing olefins affords the corresponding methyl ketones highly efficiently via a water-assisted CsC coupling between acetonyl radical and olefins.

ROLE OF THE ACETYLACETONYL RADICAL IN THE SENSITIZED PHOTOPRODUCTION OF BIS(ACETONYLACTONATO)COPPER(II)

Benzophenone-sensitized photoproduction of Cu(acac)2 generated the acetylacetonyl radical (acac.) which could be trapped as acetylacetone by hydrogen as well as by a H-atom-donating agent, or as the corresponding nitroxide with 2-nitroso-2-methylpropane,

DECOMPOSITION DU PERCARBONATE DE O,O-t-BUTYLE ET O-ISOPROPENYLE EN SOLUTION DANS DES CYCLANES

Thermolysis of O,O-t-butyl and O-isopropenyl percarbonate in cyclohexane involves free-radical acetonylation of solvent.Free radicals derived from solvent add to the percarbonate double bond and after a double β-scission reaction, cyclohexylacetone carbon dioxide and t-butoxy radicals are formed.Abstracting H atoms from the solvent, t-butoxy radicals regenerate free radicals from solvent, and the reaction becomes a chain process.Extending the study to other cycloalkanes it has been shown that the process is a general synthesis method for cycloalkylacetones.On the other hand, competitive reactions of pairs of solvents have shown that the reactivity of the substrates depends on H atom lability and on more complex phenomena like transfers between hydrocarbons and C-centred free-radicals.