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(6-tert-butyl-5-methoxy-2-methyl-4-phenyl-1H-inden-1-yl)[4-(4-tert-butylphenyl)-2-methyl-1H-inden-1-yl] dimethylsilane

Base Information Edit
  • Chemical Name:(6-tert-butyl-5-methoxy-2-methyl-4-phenyl-1H-inden-1-yl)[4-(4-tert-butylphenyl)-2-methyl-1H-inden-1-yl] dimethylsilane
  • CAS No.:1417536-81-2
  • Molecular Formula:C43H50OSi
  • Molecular Weight:610.955
  • Hs Code.:
  • Mol file:1417536-81-2.mol
(6-tert-butyl-5-methoxy-2-methyl-4-phenyl-1H-inden-1-yl)[4-(4-tert-butylphenyl)-2-methyl-1H-inden-1-yl] dimethylsilane

Synonyms:(6-tert-butyl-5-methoxy-2-methyl-4-phenyl-1H-inden-1-yl)[4-(4-tert-butylphenyl)-2-methyl-1H-inden-1-yl] dimethylsilane

Suppliers and Price of (6-tert-butyl-5-methoxy-2-methyl-4-phenyl-1H-inden-1-yl)[4-(4-tert-butylphenyl)-2-methyl-1H-inden-1-yl] dimethylsilane
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Chemical Property of (6-tert-butyl-5-methoxy-2-methyl-4-phenyl-1H-inden-1-yl)[4-(4-tert-butylphenyl)-2-methyl-1H-inden-1-yl] dimethylsilane Edit
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Technology Process of (6-tert-butyl-5-methoxy-2-methyl-4-phenyl-1H-inden-1-yl)[4-(4-tert-butylphenyl)-2-methyl-1H-inden-1-yl] dimethylsilane

There total 9 articles about (6-tert-butyl-5-methoxy-2-methyl-4-phenyl-1H-inden-1-yl)[4-(4-tert-butylphenyl)-2-methyl-1H-inden-1-yl] dimethylsilane 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:
7-(4-tert-butylphenyl)-2-methyl-1H-indene; With n-butyllithium; In diethyl ether; hexane; at -78 - 20 ℃; for 1h;
With copper(l) cyanide; In diethyl ether; at 20 ℃;
(6-tert-butyl-5-methoxy-2-methyl-4-phenyl-1H-inden-1-yl)(chloro)dimethylsilane; In diethyl ether; at -70 ℃;
Guidance literature:
Multi-step reaction with 6 steps
1.1: Eaton′s Reagent / 2 h / 50 - 55 °C / Cooling with ice
2.1: sodium acetate trihydrate; tetraethylammonium iodide; bromine / dichloromethane; water / 1.08 h / 5 °C
3.1: sodium carbonate; palladium diacetate; triphenylphosphine / water; 1,2-dimethoxyethane / 12 h / Reflux
4.1: sodium tetrahydroborate / tetrahydrofuran; methanol / 2.5 h / 5 °C
5.1: n-butyllithium / tetrahydrofuran; toluene; hexane / 16 h / -20 - 60 °C
5.2: 1 h / 60 °C
6.1: n-butyllithium / hexane; diethyl ether / 1 h / -78 - 20 °C
6.2: 20 °C
6.3: -70 °C
With sodium tetrahydroborate; n-butyllithium; Eaton′s Reagent; tetraethylammonium iodide; bromine; palladium diacetate; sodium acetate trihydrate; sodium carbonate; triphenylphosphine; In tetrahydrofuran; methanol; 1,2-dimethoxyethane; diethyl ether; hexane; dichloromethane; water; toluene;
Guidance literature:
Multi-step reaction with 5 steps
1.1: sodium acetate trihydrate; tetraethylammonium iodide; bromine / dichloromethane; water / 1.08 h / 5 °C
2.1: sodium carbonate; palladium diacetate; triphenylphosphine / water; 1,2-dimethoxyethane / 12 h / Reflux
3.1: sodium tetrahydroborate / tetrahydrofuran; methanol / 2.5 h / 5 °C
4.1: n-butyllithium / tetrahydrofuran; toluene; hexane / 16 h / -20 - 60 °C
4.2: 1 h / 60 °C
5.1: n-butyllithium / hexane; diethyl ether / 1 h / -78 - 20 °C
5.2: 20 °C
5.3: -70 °C
With sodium tetrahydroborate; n-butyllithium; tetraethylammonium iodide; bromine; palladium diacetate; sodium acetate trihydrate; sodium carbonate; triphenylphosphine; In tetrahydrofuran; methanol; 1,2-dimethoxyethane; diethyl ether; hexane; dichloromethane; water; toluene;
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