Conditions | Yield |
---|---|
With potassium hexamethylsilazane In neat liquid at 30℃; for 2h; Schlenk technique; Inert atmosphere; chemoselective reaction; | 99% |
With chlorine[2-(4,5-dihydro-1H-imidazol-2-yl)-6-methoxypyridine](pentamethylcyclopentadienyl)iridium(III) chloride In tetrahydrofuran at 20℃; for 8h; Schlenk technique; chemoselective reaction; | 90% |
With air; hydrido(triphenylphosphine)copper(I) hexamer In benzene for 1.5h; Ambient temperature; | 76% |
Conditions | Yield |
---|---|
In benzene-d6 at 20℃; for 24h; Cooling with liquid nitrogen; Sealed tube; Inert atmosphere; | A n/a B 97% C 74% |
Conditions | Yield |
---|---|
In benzene-d6 at 20℃; for 2h; Cooling with liquid nitrogen; Sealed tube; Inert atmosphere; | 95% |
methanol
sodium methylate
diphenylsilyl dichloride
dimethoxy(diphenyl)silane
Conditions | Yield |
---|---|
In diethyl ether at 40℃; for 4h; Time; Temperature; Inert atmosphere; | 94.16% |
Conditions | Yield |
---|---|
In methanol; diethyl ether at 40℃; for 4h; Temperature; Concentration; Solvent; Inert atmosphere; | 94.16% |
Conditions | Yield |
---|---|
In diethyl ether at 40℃; for 3.5h; Inert atmosphere; | 78.3% |
tetrabutyl phosphonium bromide
diphenylsilyl dichloride
dimethoxy(diphenyl)silane
Conditions | Yield |
---|---|
In sulfolane | 78% |
tetramethylorthosilicate
[diphenylmanganese]
A
phenyl trimethylsiloxane
B
dimethoxy(diphenyl)silane
Conditions | Yield |
---|---|
In toluene at 80℃; for 2h; Inert atmosphere; Schlenk technique; | A 12% B 77% |
tetramethylorthosilicate
A
phenyl trimethylsiloxane
B
dimethoxy(diphenyl)silane
Conditions | Yield |
---|---|
In toluene at 80℃; for 2h; Inert atmosphere; Schlenk technique; | A 12% B 77% |
Conditions | Yield |
---|---|
Stage #1: methanol; benzene With pyridine; tetrachlorosilane for 0.333333h; cooling; Stage #2: at 70 - 80℃; for 5h; | 71% |
(OC)4Mn(μ-SiPh2)(μ-H)Pt(PPh3)2
A
tetracarbonylhydrido(triphenylphosphine)manganese
(OC)4Mn(μ-PPh2)(μ-H)PtPh(PPh3)
C
dimethoxy(diphenyl)silane
Conditions | Yield |
---|---|
With methanol In benzene byproducts: H2; addn. of methanol to soln. of (OC)4Mn(SiPh2)(H)Pt(PPh3), stirring for ca. 8 h, standing overnight (dry and oxygen-free conditions); isolation of crystals formed, elem. anal.; | A <1 B 50% C n/a |
(OC)4Mn(μ-SiMe2)(μ-H)Pt(PPh3)2
A
tetracarbonylhydrido(triphenylphosphine)manganese
(OC)4Mn(μ-PPh2)(μ-H)PtPh(PPh3)
C
dimethoxy(diphenyl)silane
Conditions | Yield |
---|---|
With methanol In benzene byproducts: H2; addn. of methanol to soln. of (OC)4Mn(SiMe2)(H)Pt(PPh3), stirring for ca. 5 h, standing overnight (dry and oxygen-free conditions); isolation of crystals formed, elem. anal.; | A <1 B 50% C n/a |
dichlorodimethoxysilane
dimethoxy(diphenyl)silane
Conditions | Yield |
---|---|
With C6H5Cl; Na In toluene at 110°C;; | |
With sodium; chlorobenzene In toluene at 110°C;; |
methanol
diphenylsilane
A
diphenyl(methoxy)silane
B
dimethoxy(diphenyl)silane
Conditions | Yield |
---|---|
With [(PNP)(H)Ir=SiPh2][B(C6F5)4] In bromobenzene-d5 at 20℃; Inert atmosphere; | A 70 %Spectr. B 22 %Spectr. |
With tetrakis(trimethylphosphine)nickel(0) In benzene-d6 at 80℃; for 20h; Inert atmosphere; Glovebox; Schlenk technique; |
Methyltrimethoxysilan
diphenylsilanediol
A
methoxydiphenylsilanol
B
dimethoxy(diphenyl)silane
Conditions | Yield |
---|---|
In tetrahydrofuran at 23℃; for 24h; |
Methyltrimethoxysilan
diphenylsilanediol
A
1,1,5,5-tetramethoxy-1,5-dimethyl-3,3-diphenyltrisiloxane
B
dimethoxy(diphenyl)silane
Conditions | Yield |
---|---|
With 1,8-diazabicyclo[5.4.0]undec-7-ene In tetrahydrofuran at -20℃; for 5h; |
phenyl trimethylsiloxane
phenylmagnesium chloride
dimethoxy(diphenyl)silane
Conditions | Yield |
---|---|
In tetrahydrofuran at 60 - 70℃; for 1h; Inert atmosphere; | 200.2 g |
Conditions | Yield |
---|---|
With magnesium In tetrahydrofuran; toluene at 60 - 70℃; for 1h; Concentration; Inert atmosphere; | 232 g |
Conditions | Yield |
---|---|
With C21H41N3NiP2 In N,N-dimethyl-formamide at 20 - 60℃; for 36h; Sealed tube; | |
With 1,10-Phenanthroline; manganese(II) acetate In [D3]acetonitrile at 80℃; for 24h; Catalytic behavior; Reagent/catalyst; |
carbon dioxide
diphenylsilane
A
diphenyldiformoxysilane
B
dimethoxy(diphenyl)silane
Conditions | Yield |
---|---|
With 1,10-Phenanthroline; zinc diacetate In [D3]acetonitrile at 80℃; under 1875.19 Torr; for 24h; Catalytic behavior; Kinetics; Temperature; Autoclave; Glovebox; |
dideuteriodiphenylsilane
A
diphenyldiformoxysilane
B
dimethoxy(diphenyl)silane
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: zinc diacetate; 1,10-Phenanthroline / [D3]acetonitrile / 0.5 h / 25 °C 2: zinc diacetate; 1,10-Phenanthroline / [D3]acetonitrile / 24 h / 80 °C / 1875.19 Torr / Autoclave; Glovebox View Scheme |
dideuteriodiphenylsilane
dimethoxy(diphenyl)silane
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: zinc diacetate; 1,10-Phenanthroline / [D3]acetonitrile / 0.5 h / 25 °C 2: 1,10-Phenanthroline; manganese(II) acetate / [D3]acetonitrile / 24 h / 80 °C View Scheme |
Conditions | Yield |
---|---|
With boron trifluoride diethyl etherate at 20℃; for 48h; Inert atmosphere; | 99% |
With lithium hexafluorophosphate at 200℃; for 0.5h; | 98% |
With lithium hexafluorophosphate In various solvent(s) at 200℃; for 0.5h; | 98% |
With boron trifluoride diethyl etherate at 40℃; for 24h; | 7.57 g |
dimethoxy(diphenyl)silane
4-methyl-benzaldehyde
4-methylphenyl(phenyl)methanol
Conditions | Yield |
---|---|
Stage #1: dimethoxy(diphenyl)silane; 4-methyl-benzaldehyde With 1,1'-bis-(diphenylphosphino)ferrocene; (PPh3)3CuF In N,N-dimethyl-formamide at 40℃; for 1h; Stage #2: With tetrabutyl ammonium fluoride In tetrahydrofuran; N,N-dimethyl-formamide at 20℃; for 0.166667h; | 99% |
dimethoxy(diphenyl)silane
Conditions | Yield |
---|---|
at 25 - 120℃; Temperature; Inert atmosphere; | 98.1% |
dimethoxy(diphenyl)silane
methylmagnesium bromide
methoxy(methyl)diphenylsilane
Conditions | Yield |
---|---|
In diethyl ether at 0 - 20℃; for 12h; | 98% |
In diethyl ether at 0 - 20℃; for 12h; Inert atmosphere; | 98% |
Conditions | Yield |
---|---|
With water; sodium hydroxide at 20℃; for 24h; | 98% |
Conditions | Yield |
---|---|
With tris(pentafluorophenyl)borate In toluene at 20℃; for 13h; Inert atmosphere; | 96% |
dimethoxy(diphenyl)silane
ethylmagnesium bromide
ethyl(methoxy)(diphenyl)silane
Conditions | Yield |
---|---|
In diethyl ether at 0 - 20℃; for 12h; Inert atmosphere; | 95% |
Conditions | Yield |
---|---|
With sodium hydroxide; palladium diacetate at 60℃; for 6h; Hiyama reaction; | 93% |
Conditions | Yield |
---|---|
With sodium hydroxide; palladium diacetate at 60℃; for 6h; Hiyama reaction; | 92% |
Conditions | Yield |
---|---|
Stage #1: 2-naphthyl trifluoromethyl ketone; dimethoxy(diphenyl)silane With CuF-(R)-DTBM-SEGPHOS In toluene at 70℃; for 37h; Stage #2: With tetrabutyl ammonium fluoride In tetrahydrofuran; toluene at 20℃; | 91% |
dimethoxy(diphenyl)silane
allylmagnesium bromide
methoxydiphenyl(prop-2-enyl)silane
Conditions | Yield |
---|---|
In diethyl ether at 0 - 20℃; for 12h; | 90% |
In diethyl ether at 0 - 20℃; for 12h; Inert atmosphere; | 90% |
In diethyl ether at 0 - 20℃; for 2.5h; | 82% |
In diethyl ether | 82% |
dimethoxy(diphenyl)silane
4-methyl-3-pentenylmagnesium bromide
C19H24OSi
Conditions | Yield |
---|---|
In diethyl ether at 0℃; for 1h; Inert atmosphere; | 90% |
dimethoxy(diphenyl)silane
phenylmagnesium bromide
methoxy-triphenyl-silane
Conditions | Yield |
---|---|
In diethyl ether at 0 - 20℃; for 12h; Inert atmosphere; | 90% |
dimethoxy(diphenyl)silane
sodium 4-methylbenzenesulfinate
4-Methylbiphenyl
Conditions | Yield |
---|---|
With tetrabutyl ammonium fluoride; palladium dichloride In tetrahydrofuran at 70℃; for 3h; Hiyama Coupling; | 90% |
Conditions | Yield |
---|---|
With bis(benzonitrile)palladium(II) dichloride; camphor-10-sulfonic acid; tetrabutyl ammonium fluoride In tetrahydrofuran at 50℃; for 3h; Hiyama Coupling; | 90% |
Conditions | Yield |
---|---|
Stage #1: 4-bromo-aniline With hydrogenchloride In water at 0 - 5℃; Stage #2: With sodium tetrafluoroborate; sodium nitrite In water at 5℃; for 0.166667h; Stage #3: dimethoxy(diphenyl)silane With methanol; palladium diacetate at 25℃; for 6h; Hiyama coupling; chemoselective reaction; | 89% |
1,1,3,3-Tetramethyldisiloxane
dimethoxy(diphenyl)silane
1,1,5,5-tetramethyl-3,3-diphenyl-trisiloxane
Conditions | Yield |
---|---|
Stage #1: dimethoxy(diphenyl)silane With sulfuric acid for 0.166667h; Stage #2: 1,1,3,3-Tetramethyldisiloxane for 28h; | 88.97% |
Conditions | Yield |
---|---|
Stage #1: p-toluidine With hydrogenchloride In water at 0 - 5℃; Stage #2: With sodium tetrafluoroborate; sodium nitrite In water at 5℃; for 0.166667h; Stage #3: dimethoxy(diphenyl)silane With methanol; palladium diacetate at 25℃; for 6h; Hiyama coupling; | 86% |
Stage #1: p-toluidine With hydrogenchloride; sodium nitrite In water at 0 - 5℃; Stage #2: With sodium tetrafluoroborate In water for 0.166667h; Stage #3: dimethoxy(diphenyl)silane With tetrabutyl ammonium fluoride; palladium diacetate In water at 25℃; for 6h; Hiyama Coupling; |
pyrrolidine
dimethoxy(diphenyl)silane
methoxy(diphenyl)pyrrolidinosilane
Conditions | Yield |
---|---|
Stage #1: pyrrolidine With n-butyllithium In hexane; pentane at -30 - 0℃; for 1h; Stage #2: dimethoxy(diphenyl)silane In hexane at -60 - 20℃; for 20h; | 86% |
dimethoxy(diphenyl)silane
Conditions | Yield |
---|---|
Stage #1: 2,2''-dibromo-5'-(2-bromo-5-fluorophenyl)-5,5''-difluoro-1,1':3',1''-terphenyl With tert.-butyl lithium In diethyl ether; pentane at -125 - 20℃; for 1.66667h; Inert atmosphere; Stage #2: dimethoxy(diphenyl)silane In diethyl ether; pentane at -125 - 20℃; for 12.25h; Inert atmosphere; | 86% |
dimethoxy(diphenyl)silane
3,5-dimethylaminoaniline
3,5-dimethylbiphenyl
Conditions | Yield |
---|---|
Stage #1: 3,5-dimethylaminoaniline With hydrogenchloride In water at 0 - 5℃; Stage #2: With sodium tetrafluoroborate; sodium nitrite In water at 5℃; for 0.166667h; Stage #3: dimethoxy(diphenyl)silane With methanol; palladium diacetate at 25℃; for 6h; Hiyama coupling; | 85% |
dimethoxy(diphenyl)silane
lithium trimethylsilylacetylenide
Conditions | Yield |
---|---|
In tetrahydrofuran at 20℃; for 0.5h; Inert atmosphere; | 85% |
Conditions | Yield |
---|---|
With tris(pentafluorophenyl)borate In toluene for 3h; | 83% |
dimethoxy(diphenyl)silane
2-hydroxymethyl-1-(3-hydroxypropyl)aziridine
Conditions | Yield |
---|---|
With sodium methylate for 12h; Ambient temperature; | 81% |
dimethoxy(diphenyl)silane
4-phenyl-N-(quinolin-8-yl)butanamide
Conditions | Yield |
---|---|
With copper (II)-fluoride; water; palladium diacetate In tetrahydrofuran at 100℃; for 24h; Sealed tube; | 81% |
The Benzene,1,1'-(dimethoxysilylene)bis-, with the CAS registry number 6843-66-9, has the IUPAC name of dimethoxy(diphenyl)silane. For being a kind of colorless clear liquid, it is sensitive to moisture, with the product categories including Dialkoxysilanes; Functional Materials; Si (Classes of Silicon Compounds); Silane Coupling Agents; Silane Coupling Agents (Intermediates); Si-O Compounds; Phenyl Silanes. As to its usage, it is usually applied in the propylene polymerization reaction.
The characteristics of this chemical are as follows: (1)ACD/LogP: 3.86; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): 3.86; (4)ACD/LogD (pH 7.4): 3.86; (5)ACD/BCF (pH 5.5): 502.98; (6)ACD/BCF (pH 7.4): 502.98; (7)ACD/KOC (pH 5.5): 2987.93; (8)ACD/KOC (pH 7.4): 2987.93; (9)#H bond acceptors: 2; (10)#H bond donors: 0; (11)#Freely Rotating Bonds: 4; (12)Polar Surface Area: 18.46; (13)Index of Refraction: 1.543; (14)Molar Refractivity: 72.95 cm3; (15)Molar Volume: 231.3 cm3; (16)Polarizability: 28.92 ×10-24 cm3; (17)Surface Tension: 33.8 dyne/cm; (18)Density: 1.05 g/cm3; (19)Flash Point: 159.1 °C; (20)Enthalpy of Vaporization: 50.46 kJ/mol; (21)Boiling Point: 286.6 °C at 760 mmHg; (22)Vapour Pressure: 0.00451 mmHg at 25°C; (23)Exact Mass: 244.091956; (24)MonoIsotopic Mass: 244.091956; (25)Topological Polar Surface Area: 18.5; (26)Heavy Atom Count: 17; (27)Complexity: 196; (28)Covalently-Bonded Unit Count: 1.
When you are dealing with this chemical, you should be cautious. This is a irritating to skin and may cause inflammation to the skin or other mucous membranes, so you should wear suitable gloves. After contact with skin, wash immediately with plenty of ... (to be specified by the manufacturer).
In addition, you could convert the following datas into the molecular structure:
(1)Canonical SMILES: CO[Si](C1=CC=CC=C1)(C2=CC=CC=C2)OC
(2)InChI: InChI=1S/C14H16O2Si/c1-15-17(16-2,13-9-5-3-6-10-13)14-11-7-4-8-12-14/h3-12H,1-2H3
(3)InChIKey: AHUXYBVKTIBBJW-UHFFFAOYSA-N
Below are the toxicity information of this chemical:
Organism | Test Type | Route | Reported Dose (Normalized Dose) | Effect | Source |
---|---|---|---|---|---|
rat | LC | inhalation | > 42mg/m3/4H (42mg/m3) | National Technical Information Service. Vol. OTS0539962, |
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