732-66-1

Usage

Molecular structure

A complex chemical compound with a tricyclic ring system and a total of 16 carbon atoms and 5 double bonds.

Hydroxyl group

Contains a hydroxyl (-OH) group attached to one of the carbon atoms in the ring system.

Ethyl group

Has an ethyl (-CH2CH3) group attached to one of the carbon atoms in the ring system.

Potential applications

Likely to have diverse applications in various fields such as pharmaceuticals, materials science, and organic synthesis.

Physical properties

Unique physical properties due to its complex structure (exact properties not provided in the material).

Chemical properties

Unique chemical properties due to its complex structure (exact properties not provided in the material).

Further research

Additional research and analysis are necessary to fully understand the properties and potential uses of 1-[tricyclo[8.2.2.2~4,7~]hexadeca-1(12),4,6,10,13,15-hexaen-5-yl]ethanol.

Upstream product

• 1633-22-3 [2.2]Paracyclophan 
• 735-65-9 2-bromo-1-tricyclo[8.2.2.24,7]hexadeca-1⁽¹³⁾,4,6,10⁽¹⁴⁾,11,15-hexaen-5-yl-ethanone 
• 10029-00-2 4-acetyl[2.2]paracyclophane 

Relevant academic research and scientific papers

An improved synthesis of (S)-(+)- and (R)-(-)-4-ethenyl[2.2]paracyclophane

The resolution of the 4-acetyl[2.2]paracyclophane by the SAMP-hydrazone method is described. A new, short, high yield synthesis of both enantiomers (S)-(+)- and (R)-(-)-4-ethenyl[2.2]paracyclophane is reported. Copyright (C) 2000 Elsevier Science Ltd.

A practical kinetic resolution of 4-acetyl[2.2]paracyclophane

The kinetic resolution of 4-acetyl[2.2]paracyclophane has been realized by borane reduction in the presence of a CBS catalyst. The structure of the two diastereomeric alcohol products has been established. The ketone was recovered in the more than 99% e.e. at 69% conversion.

Multigram-Scale Kinetic Resolution of 4-Acetyl[2.2]Paracyclophane via Ru-Catalyzed Enantioselective Hydrogenation: Accessing [2.2]Paracyclophanes with Planar and Central Chirality

[2.2]Paracyclophane (PCP) derivatives have been promising platforms to study the element of planar chirality and through-space electronic communications in π-stacked molecular systems. To access enantiomerically pure derivatives thereof, a kinetic resolut

Functional paracyclophanes: Synthesis of [2.2] paracyclophanemethyldithiocarbonates using thione-thiol rearrangement of S,O-dithiocarbonates (benzyl Schoenberg rearrangement) at mild conditions

A pathway to benzylic [2.2]paracyclophane thiol derivatives was investigated using the benzyl Schoenberg rearrangement. Copyright