293768-77-1

Basic information

• Product Name: 4-isopropyl-2-tricyclo[8.2.2.2~4,7~]hexadeca-1(12),4,6,10,13,15-hexaen-5-yl-4,5-dihydro-1,3-oxazole
• Synonyms: 4-isopropyl-2-tricyclo[8.2.2.2~4,7~]hexadeca-1(12),4,6,10,13,15-hexaen-5-yl-4,5-dihydro-1,3-oxazole
• CAS NO: 293768-77-1
• Molecular Formula: C₂₂H₂₅NO
• Molecular Weight: 319.44
• Mol File: 293768-77-1.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4-isopropyl-2-tricyclo[8.2.2.2~4,7~]hexadeca-1(12),4,6,10,13,15-hexaen-5-yl-4,5-dihydro-1,3-oxazole(CAS DataBase Reference)
• NIST Chemistry Reference: 4-isopropyl-2-tricyclo[8.2.2.2~4,7~]hexadeca-1(12),4,6,10,13,15-hexaen-5-yl-4,5-dihydro-1,3-oxazole(293768-77-1)
• EPA Substance Registry System: 4-isopropyl-2-tricyclo[8.2.2.2~4,7~]hexadeca-1(12),4,6,10,13,15-hexaen-5-yl-4,5-dihydro-1,3-oxazole(293768-77-1)

Safety Data

• Hazardous Substances Data: 293768-77-1(Hazardous Substances Data)

Upstream product

• 293768-76-0 4-(1‘-hydroxy-3’-methylbutan-2’-yl)[2.2]paracyclophane carboxamide 
• 20586-49-6 [2.2]paracyclophane-4-carboxylic acid 
• 108869-37-0 [2.2]paracyclophane-4-carboxylic acid chloride 
• 1908-61-8 4-bromo[2.2]paracyclophane 
• 1633-22-3 [2.2]Paracyclophan 

Relevant articles and documents

Novel N,S- and N,Se-planar chiral [2,2]paracyclophane ligands: Synthesis and application in Pd-catalyzed allylic alkylation

Novel N,S- and N,Se-ligands with planar chirality derived from [2.2]paracyclophane have been synthesized and applied in palladium-catalyzed allylic alkylation reaction, in which ligands 5 and 9 with the two substituents at benzylic and benzene ring positi

[2.2]Paracyclophanes with N-Heterocycles as Ligands for Mono- and Dinuclear Ruthenium(II) Complexes

[2.2]Paracyclophane, with its unique structure, allows the design of unusual 3D structures by functionalization of this rigid and stable hydrocarbon scaffold. Therefore different mono- and homodisubstituted [2.2]paracyclophanes with pyridyl, pyrimidyl and oxazolinyl substituents were developed in order to evaluate their ability as bridging ligands for two ruthenium centres. With the successfully synthesized [2.2]paracyclophane-based N-donor functions, the cycloruthenation reaction using [RuCl2(p-cymene)]2 as precursor was explored. Compared to 2-phenylpyridine, the [2.2]paracyclophane derivative is clearly inferior in the cycloruthenation reaction, resulting in poor yields for the neutral complexes. By addition of KPF6, the cationic complexes can be obtained in good yields and are formed diastereoselectively in case of a pyridyl substituent, resulting in only one diastereomer for dinuclear ruthenium complexes of bispyridyl-substituted [2.2]paracyclophanes as bridging ligands.