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5-(2,4,6-triisopropylphenyl)-5-{2,4,6-tris{bis(trimethylsilyl)methyl}phenyl}-1,2,3,4,5-tetraselenastannolane

Base Information
  • Chemical Name:5-(2,4,6-triisopropylphenyl)-5-{2,4,6-tris{bis(trimethylsilyl)methyl}phenyl}-1,2,3,4,5-tetraselenastannolane
  • CAS No.:138423-63-9
  • Molecular Formula:C42H82Se4Si6Sn
  • Molecular Weight:1190.18
  • Hs Code.:
5-(2,4,6-triisopropylphenyl)-5-{2,4,6-tris{bis(trimethylsilyl)methyl}phenyl}-1,2,3,4,5-tetraselenastannolane

Synonyms:5-(2,4,6-triisopropylphenyl)-5-{2,4,6-tris{bis(trimethylsilyl)methyl}phenyl}-1,2,3,4,5-tetraselenastannolane

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Chemical Property of 5-(2,4,6-triisopropylphenyl)-5-{2,4,6-tris{bis(trimethylsilyl)methyl}phenyl}-1,2,3,4,5-tetraselenastannolane
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Technology Process of 5-(2,4,6-triisopropylphenyl)-5-{2,4,6-tris{bis(trimethylsilyl)methyl}phenyl}-1,2,3,4,5-tetraselenastannolane

There total 9 articles about 5-(2,4,6-triisopropylphenyl)-5-{2,4,6-tris{bis(trimethylsilyl)methyl}phenyl}-1,2,3,4,5-tetraselenastannolane which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With 1,8-diazabicyclo(5.4.0)-7-undecene; In tetrahydrofuran; addn. of THF to a mixture of dihydrostannane and Se; immediate addn. of 1,8-diazabicyclo(5.4.0)-7-undecene at room temp. in one portion; stirring, 10h;; chromy. of residue obtained by filtration of excess Se (DCC, hexane); further purification of main fraction by GPLC; recrystn. from ethanol-chloroform; elem. anal.;;
DOI:10.1021/om00028a059
Guidance literature:
With tert.-butyl lithium; In tetrahydrofuran; diethyl ether; pentane; Ar-atmosphere; treatment of Si-compd. (in THF) with t-BuLi (in pentane) at -70°C, SnCl2 addn. (in ether), stirring (-65°C, 1.5 h),addn. of mixt. of i-Pr-aryl and t-BuLi (in THF), addn. of excess Se (-7 0°C), warming to room temp.; evapn., chromy. (SiO2);
DOI:10.1016/0022-328X(95)00334-M
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