Bicyclo[4.2.0]octa-1,3,5-trien-7-one, with the CAS number 3469-06-5, is an organic compound characterized by its unique bicyclic structure, which consists of two fused cyclobutane rings. This compound features a conjugated system of double bonds, contributing to its reactivity and potential applications in organic synthesis. The presence of a ketone functional group at the 7-position enhances its electrophilic character, making it a useful intermediate in various chemical reactions. Bicyclo[4.2.0]octa-1,3,5-trien-7-one is typically a colorless to pale yellow liquid or solid, depending on its purity and conditions. Its molecular structure allows for interesting stereochemical properties and reactivity patterns, particularly in cycloaddition reactions and as a precursor for more complex organic molecules. The compound's stability and reactivity can be influenced by factors such as temperature and solvent, making it a subject of interest in both academic and industrial chemistry.

bicyclo[4.2.0]octa-1,3,5-trien-7-one

Benzocyclobuten-1(2h)-one is an alkanoic acid that has been shown to have anticancer activity. It can be synthesized by the reaction of sodium salts and benzoyl chloride in a solvent, such as dichloromethane. The synthesis is efficient and can be done in a short period of time. The product is purified by recrystallization, followed by washing with water. The reaction products are functional groups, which are characterized by their ability to react with other compounds or function as hydrogen acceptors. Benzocyclobuten-1(2h)-one has three nitrogen atoms and one carbonyl group.

CAS 3469-06-5: bicyclo[4.2.0]octa-1,3,5-trien-7-one

Benzocyclobuten-1(2h)-one

Ref: 3D-FB34084

Benzocyclobutenone

Ref: IN-DA00C6LS

Benzocyclobutenone

Ref: 54-OR906275

Bicyclo[4.2.0]octa-1,3,5-trien-7-one

Ref: 10-F079402