88738-08-3

Usage

Uses

Used in Organic Synthesis:
(4-CHLORO-PHENYL)-(5-HYDROXY-CYCLOPENT-1-ENYL)-METHANONE is used as a key intermediate in the synthesis of various organic compounds. Its structural features allow for further functionalization and modification, making it a valuable building block in the development of new molecules with specific properties and applications.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (4-CHLORO-PHENYL)-(5-HYDROXY-CYCLOPENT-1-ENYL)-METHANONE is used as a potential drug candidate for therapeutic applications. Its structure indicates that it may possess biological activity, which could be harnessed for the treatment of various medical conditions. However, further research and testing are required to fully understand its properties and potential uses in this context.
Used as a Precursor in Synthesis:
(4-CHLORO-PHENYL)-(5-HYDROXY-CYCLOPENT-1-ENYL)-METHANONE may also serve as a precursor or intermediate in the synthesis of other organic compounds. Its unique combination of functional groups can be utilized to create a diverse range of molecules with different properties and applications, further expanding its utility in the chemical and pharmaceutical industries.

Upstream product

• 88738-05-0 7-(4-chlorophenylmethylene)-2,3-diazabicyclo[2.2.1]hept-2-ene 
• 871463-63-7 2-(4-chloro-phenyl)-cyclohex-3-ene-1,2-diol 

Relevant academic research and scientific papers

Bifunctional polymeric organocatalysts and their application in the cooperative catalysis of Morita-Baylis-Hillman reactions

A series of soluble, noncross-linked polystyrene-supported tri-phenylphosphane and 4-dimethylaminopyridine reagents were prepared. Some of these polymeric reagents contained either alkyl alcohol or phenol groups on the polymer backbone. The use of these materials as organocatalysts in a range of Morita-Baylis-Hillman reactions indicated that hydroxyl groups could participate in the reactions and accelerate product formation. In the cases examined, phenol groups were more effective than alkyl alcohol groups for catalyzing the reactions. This article is one of the first reports of the synthesis and use of non-natural, bifunctional polymeric reagents for use in organic synthesis in which both functional groups can cooperatively participate in the catalysis of reactions.

Influence of Michael acceptor stereochemistry on intramolecular Morita-Baylis-Hillman reactions

A study of the effect of Michael acceptor stereochemistry on the efficiency of intramolecular Morita-Baylis-Hillman (MBH) reactions has been performed. The reactions were catalyzed by a phosphine, and the reaction substrates studied were enones containing

SOME UNUSUAL REACTIONS OF MOLECULAR OXYGEN WITH BICYCLIC DIAZENES WHICH TYPICALLY SERVE AS PRECURSORS TO ALKYLIDENECYCLOPENTANE-1,3-DIYLS; PEROXIDE FORMATION

The reaction of a series of substituted bicyclic diazenes with oxygen was investigated.Three types of products result, namely ketoalcohols 2b-f, ketoaldehydes 4e-g and dioxolanes 3e-g.The potential intermediacy of an endoperoxide 5f is considered.