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CAS No.: | 35692-30-9 |
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Name: | (p-Chlorophenyl)Trimethoxysilane |
Article Data: | 3 |
Molecular Structure: | |
Formula: | C9H13ClO3Si |
Molecular Weight: | 232.739 |
Synonyms: | (4-chloro-phenyl)-trimethoxy-silane;trimethoxy(4-chlorophenyl)silane; |
Density: | 1.13±0.1 g/cm3(Predicted) |
Boiling Point: | 214.6±23.0 °C(Predicted) |
PSA: | 27.69000 |
LogP: | 1.42510 |
Conditions | Yield |
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With tris(dibenzylideneacetone)dipalladium (0); N-ethyl-N,N-diisopropylamine; tris-(o-tolyl)phosphine In N,N-dimethyl-formamide at 20℃; silylation; |
tetramethylorthosilicate
(4-chlorophenyl)trimethoxysilane
Conditions | Yield |
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In tetrahydrofuran at -30 - 20℃; for 13h; Inert atmosphere; | |
In tetrahydrofuran at -30 - 20℃; for 13h; |
1-methylindole
(4-chlorophenyl)trimethoxysilane
2-(4-chlorophenyl)-1-methyl-2-phenyl-1H-indole
Conditions | Yield |
---|---|
With tetrabutyl ammonium fluoride; palladium diacetate; acetic acid; silver(l) oxide In tetrahydrofuran; ethanol at 20℃; Inert atmosphere; regioselective reaction; | 93% |
(4-chlorophenyl)trimethoxysilane
Conditions | Yield |
---|---|
With copper(l) iodide; tetrakis(triphenylphosphine) palladium(0); tetrabutyl ammonium fluoride In tetrahydrofuran at 60℃; for 1.5h; Hiyama coupling; Inert atmosphere; | 92% |
Conditions | Yield |
---|---|
With potassium fluoride; 5,11,17,23-tetra-t-butyl-25,26,27,28-tetrahydroxycalix-4-arene; copper(ll) bromide; magnesium chloride for 8h; Inert atmosphere; Heating; | 92% |
(4-chlorophenyl)trimethoxysilane
benzenesulfonyl chloride
4'-biphenyl chloride
Conditions | Yield |
---|---|
With tris-(dibenzylideneacetone)dipalladium(0); tetrabutyl ammonium fluoride In N,N-dimethyl-formamide; acetonitrile at 100℃; for 3h; Hiyama Coupling; Inert atmosphere; Green chemistry; | 86% |
S-methyl-S-(p-tolyl)sulfoximine
(4-chlorophenyl)trimethoxysilane
N-(4-chloro)phenyl-S-(4-methyl)phenyl-S-methylsulfoximine
Conditions | Yield |
---|---|
With copper(l) iodide; tetrabutyl ammonium fluoride; oxygen In dichloromethane at 20℃; for 12h; Schlenk technique; Green chemistry; | 84% |
N-(2-pyrimidyl)indole
(4-chlorophenyl)trimethoxysilane
2-(4-chlorophenyl)-1-(pyrimidin-2-yl)-1H-indole
Conditions | Yield |
---|---|
With copper (II)-fluoride; silver hexafluoroantimonate; [ruthenium(II)(η6-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]2 In water at 140℃; for 20h; Hiyama Coupling; Inert atmosphere; Green chemistry; | 81% |
With copper (II)-fluoride; oxygen; cobalt(III) acetylacetonate In toluene at 160℃; under 760.051 Torr; for 24h; Hiyama Coupling; Sealed tube; | 63% |
(3-chlorophenyl)(imino)(methyl)-λ6-sulfanone
(4-chlorophenyl)trimethoxysilane
Conditions | Yield |
---|---|
With copper(l) iodide; tetrabutyl ammonium fluoride; oxygen In dichloromethane at 20℃; for 12h; Schlenk technique; Green chemistry; | 80% |
carbon monoxide
(4-chlorophenyl)trimethoxysilane
aniline
4-chlorobenzanilide
Conditions | Yield |
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With copper (II)-fluoride; bis(triphenylphosphine)palladium(II) dichloride In acetonitrile at 80℃; under 760.051 Torr; for 24h; Hiyama Coupling; Schlenk technique; | 80% |