97106-61-1

Basic information

• Product Name: diphenyl(2-(trimethylstannyl)phenyl)phosphane
• Synonyms: diphenyl(2-(trimethylstannyl)phenyl)phosphane
• CAS NO: 97106-61-1
• Molecular Weight: 425.097
• Mol File: 97106-61-1.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: diphenyl(2-(trimethylstannyl)phenyl)phosphane(CAS DataBase Reference)
• NIST Chemistry Reference: diphenyl(2-(trimethylstannyl)phenyl)phosphane(97106-61-1)
• EPA Substance Registry System: diphenyl(2-(trimethylstannyl)phenyl)phosphane(97106-61-1)

Safety Data

• Hazardous Substances Data: 97106-61-1(Hazardous Substances Data)

Upstream product

• 864512-14-1 2-iodophenyl 4-chlorobenzenesulfonate 
• 1213-51-0 (trimethylstannyl)diphenylphosphine 
• 129112-26-1 2-iodophenyltrifluoromethanesulfonic acid 
• 129112-25-0 2-(trifluoromethanesulfonyl)oxy-bromobenzene 
• 829-85-6 diphenylphosphane 
• 1066-45-1 trimethyltin(IV)chloride 
• 62336-24-7 (2-bromophenyl)diphenylphosphane 

Downstream Products

• 97106-63-3 diphenyl(2-(trimethylstannyl)phenyl)phosphane oxide 
• 1618100-84-7 2-Me₃SnC₆H₄P(S)Ph₂ 
• 1618100-85-8 2-Me₃SnC₆H₄P(Se)Ph₂ 
• 1618100-62-1 [Pt{κ2-2-C6H4P(Se)Ph2}2] 
• 1618100-63-2 cis-[Pd{κ2-2-C6H4P(S)Ph2}2] 
• 1618100-64-3 cis-[Pd{κ2-2-C6H4P(Se)Ph2}2] 
• 1618100-65-4 [Pd2(μ-Cl)2{κ2-2-C6H4P(S)Ph2}2] 
• 1618100-66-5 [Pd2(μ-Cl)2{κ2-2-C6H4P(Se)Ph2}2] 
• 1618100-67-6 [Pd{κ2-2-C6H4P(S)Ph2}{κ2-2-C6H4P(Se)Ph2}] 
• 1618100-71-2 [PdCl{κ2-2-C6H4P(S)Ph2}(PPh3)] 
• 1618100-76-7 [Pd{κ2-2-C6H4P(S)Ph2}(κ2-OC6H4CHvNC6H4-4-OMe)] 
• 1618100-77-8 [Pd{κ2-2-C6H4P(S)Ph2}(κ2-OC6H4CHvNC6H4-4-NO2)] 
• 1618100-78-9 [Pd{κ2-2-C6H4P(Se)Ph2}(κ2-OC6H4CHvNC6H4-4-OMe)] 
• 1618100-79-0 [Pd{κ2-2-C6H4P(S)Ph2}(κ2-OC6H4CHvNC6H4-4-NO2)] 

Relevant articles and documents

Ortho-Trialkylstannyl Arylphosphanes by C-P and C-Sn Bond Formation in Arynes

A novel and efficient approach to ortho-trialkylstannyl arylphosphanes by the reaction of arynes generated in situ with stannylated phosphanes (R3Sn-PR2) is described. Concurrent C-P and C-Sn bond formation occurs with high yields, and stannylated products are easily transformed into valuable ortho-substituted arylphosphanes. The reaction features high efficiency, good regioselectivity, and excellent practicality.