52168-00-0

Basic information

• Product Name: Silane, trimethyl[(pentafluorophenyl)ethynyl]-
• CAS NO: 52168-00-0
• Molecular Formula: C11H9F5Si
• Molecular Weight: 264.27
• Mol File: 52168-00-0.mol
• Article Data: 12

Chemical Properties

• CAS DataBase Reference: Silane, trimethyl[(pentafluorophenyl)ethynyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Silane, trimethyl[(pentafluorophenyl)ethynyl]-(52168-00-0)
• EPA Substance Registry System: Silane, trimethyl[(pentafluorophenyl)ethynyl]-(52168-00-0)

Safety Data

• Hazardous Substances Data: 52168-00-0(Hazardous Substances Data)

Upstream product

• 344-04-7 bromopentafluorobenzene 
• 1066-54-2 trimethylsilylacetylene 
• 771-61-9 2,3,4,5,6-pentafluorophenol 
• 827-15-6 1,2,3,4,5-pentafluoro-6-iodobenzene 
• 60129-85-3 Perfluorophenyl trifluoromethanesulfonate 
• 363-72-4 Pentafluorobenzene 
• 133816-00-9 phenyl(trimethylsilylethynyl)iodonium triflate 
• 145664-96-6 Perfluorophenyl 5H-3-oxaperfluoropentanesulfonate 

Downstream Products

• 149083-68-1 4-n-octyloxytetrafluorophenylacetylene 
• 1104876-31-4 Ru(CCC₆F₅)(dppe)Cp* 
• 1104876-28-9 Ru(CCC₆F₅)(dppe)Cp 
• 1030891-82-7 C₁₇H₅F₅O 
• 1030892-04-6 1-pentafluorophenyl-5-(tert-butyldimethylsilyl)-1,4-pentadiyn-3-one 
• 1058606-78-2 3-(dibromomethylene)-pentafluorophenyl-5-(tert-butyldimethylsilyl)-penta-1,4-diyne 
• 1030892-14-8 1-triisopropylsilyl-5-dibromomethylene-7-pentafluorophenyl-1,3,6-heptatriyne 
• 1190954-65-4 1-tert-butyldimethylsilyl-5-dibromomethylene-7-pentafluorophenyl-1,3,6-heptatriyne 
• 1030891-80-5 1-pentafluorophenyl-6-phenyl-hexatriyne 
• 13557-43-2 1,2-bis(pentafluorophenyl)acetylene 
• 1315381-38-4 C₃₂F₂₂ 
• 1315381-36-2 C₃₀H₁₀F₈ 
• 1381888-25-0 1-((trimethylsilyl)ethynyl)-2,3,5,6-tetrafluorobenzene 
• 66535-27-1 1,2,3,4,5-pentafluoro-6-(iodoethynyl)benzene 

Relevant articles and documents

Bis(pentafluorophenyl)-: O-carborane and its arylthio derivatives: Synthesis, electrochemistry and optical properties

Synthesis of 1,2-bis(pentafluorophenyl)-o-carborane and its arylthio-derivatives is reported. The regioselective arylthiolation was successfully achieved via nucleophilic aromatic substitution (SNAr) reaction. A series of bis(perfluoroaryl)-o-carboranes w

Systematic Experimental and Computational Studies of Substitution and Hybridization Effects in Solid-State Halogen Bonded Assemblies

A quantitative assessment of the substituent, hybridization, and crystal-packing effects on the electronic, structural, and vibrational properties of halogen bonded systems is presented. Through a combined experimental and theoretical approach employing R

Halogen bonding of (iodoethynyl)benzene derivatives in solution

Halogen bonding (XB) between (iodoethynyl)benzene donors and quinuclidine in benzene affords binding free enthalpies (δG, 298 K) between -1.1 and -2.4 kcal mol-1, with a strong LFER with the Hammett parameter σpara. The enthalpic dri