165184-83-8

Basic information

• Product Name: 1-Undecanone, 4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,11-heptadecafluoro-1-phenyl-
• CAS NO: 165184-83-8
• Molecular Formula: C17H9F17O
• Molecular Weight: 552.231
• Mol File: 165184-83-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1-Undecanone, 4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,11-heptadecafluoro-1-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Undecanone, 4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,11-heptadecafluoro-1-phenyl-(165184-83-8)
• EPA Substance Registry System: 1-Undecanone, 4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,11-heptadecafluoro-1-phenyl-(165184-83-8)

Safety Data

• Hazardous Substances Data: 165184-83-8(Hazardous Substances Data)

Usage

Common uses

Insect repellent, production of perfumes and flavorings, chemical intermediate in manufacturing other compounds

Effective against

Mosquitoes, ticks, flies, and other insect species

Safety

Non-toxic to humans and animals

Environmental impact

Relatively environmentally friendly, low toxicity level

Physical properties

Not provided in the material

Chemical properties

Not provided in the material

Upstream product

• 2043-53-0 2-(n-perfluorooctyl)ethyl iodide 
• 201230-82-2 carbon monoxide 
• 960-16-7 tributylphenylstannane 
• 606935-04-0 4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,11-Heptadecafluoro-1-phenyl-undecan-1-ol 
• 34598-33-9 4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,11-heptadecafluoroundecanoic acid 
• 100-52-7 benzaldehyde 
• 21652-57-3 1-bromo-1,1,2,2-tetrahydroperfluorodecane 

Relevant articles and documents

Palladium catalyzed coupling reactions of β-perfluoroalkyl-substituted alkyl halides with organostannanes

β-Perfluoroalkyl-substituted alkyl halides reacted with organostannanes such as allyl-, phenylethynyl-, β-phenylethenyl-, and phenyl-tributyltin in the presence of palladium-phosphine complexes to give the corresponding cross-coupling products in good yie

Enantiomeric resolution of fluorous mixture by chiral CD columns: Asymmetric reduction of a mixture of fluorous ketones

Asymmetric reduction of a mixture of four fluorous ketone analogues was carried out with (R)-oxazaborolidine as a catalyst. The fluorous mixture products were resolved by a reverse phase HPLC with chiral β-cyclodextrin column to result in good separation of the enantiomers.