15807-28-0

Upstream product

• 962-89-0 triphenyltin bromide 
• 13328-67-1 penta(p-tolyl)antimony(V) 
• 4167-90-2 lithium triphenylstannide 
• 894-09-7 iodotriphenylstannane 
• 96868-89-2 (C₆H₅)3SnC₆H₄-p-CH₂CHCH₂ 
• 96469-14-6 (C₆H₅)3SnC₆H₄-p-cyclo-C₆H₁₁ 
• 15807-57-5 (C₆H₅)3SnC₆H₄-o-CH₃ 
• 639-58-7 triphenyltin chloride 
• 4294-57-9 para-methylphenylmagnesium bromide 

Downstream Products

• 639-58-7 triphenyltin chloride 
• 595-90-4 tetraphenyltin(IV) 
• 859795-04-3 (C₆H₅)3SnC₆H₃(N(CH₃)2)NNC₆H₄Br 
• 41411-81-8 (C₆H₅)3SnC₆H₄-p-C₆H₅ 
• 96469-14-6 (C₆H₅)3SnC₆H₄-p-cyclo-C₆H₁₁ 
• 31868-28-7 (C₆H₅)3SnC₆H₄-p-N(CH₃)2 
• 2177-15-3 (C₆H₅)3SnC₆H₄-p-C₆H₄-p-CHCH₂ 
• 63243-09-4 (C₆H₅)3SnC₆H₄-p-COOH 
• 96868-89-2 (C₆H₅)3SnC₆H₄-p-CH₂CHCH₂ 
• 107278-32-0 {(C₆H₅)3SnC₆H₄-p-CH₂CH₂}2Sn(C₆H₅)2 
• 57879-99-9 (C₆H₅)3SnC₆H₄-p-C(CH₃)3 
• 106217-86-1 (C₆H₅)3SnC₆H₄-p-CH₂CH₂Sn(C₆H₅)3 
• 24344-42-1 (C₆H₅)3SnC₆H₄-m-Cl 
• 24344-43-2 (C₆H₅)3SnC₆H₄-m-Br 

Relevant academic research and scientific papers

Arylation of organotin halides with pentaarylantimony and pentaphenylbismuth

Pentaarylantimony and pentaphenylbismuth arylate oranotin halides R3SnX and R2SnX2 (R = Alk, Ar; X = Cl, Br) in toluene at room temperature to aryltin derivatives R3SnAr and R2SnArX (initial reagent molar ratio 1:1) or R2SnAr2 (2:1) in 78-95% yield.

Ueber Tetraaryl-Methan-Analoga in der Gruppe 14. II. Ph4-nSi-p-Toln und Ph4-nSn-p-Toln (n = 0 bis 4): Einfluss der p-Tolyl-Substituenten auf Struktur und NMR-chemische Verschiebungen

The title compounds have been synthesized by Li and Grignard reactions.The crystal structure of Ph3Si-p-Tol has been determined.The substitution of only one phenyl by one p-tolyl group causes only a slight deviation from the ideal S4 symmetry of Ph4Si.Gra