dichloromethylphenylsilane
1,3,5-triphenyl-1,3,5-trimethylcyclotrisiloxane
B
2,4,6,8-tetraphenyl-2,4,6,8-tetramethylcyclotetrasiloxane
Conditions | Yield |
---|---|
With pyridine; sodium hydrogencarbonate In acetone at 20℃; for 3h; | A 33% B 65.5% |
With tetrahydrofuran; lithium at 35 - 45℃; Product distribution; Mechanism; | |
With tetrahydrofuran; lithium at 35 - 45℃; Yield given. Yields of byproduct given. Title compound not separated from byproducts; |
dichloromethylphenylsilane
A
2.4.6.8.10-Pentamethyl-2.4.6.8.10-pentaphenyl-cyclopentasiloxan
1,3,5-triphenyl-1,3,5-trimethylcyclotrisiloxane
C
2,4,6,8-tetraphenyl-2,4,6,8-tetramethylcyclotetrasiloxane
D
cis-trans-cis-2,4,6,8-tetraphenyl-2,4,6,8-tetramethylcyclotetrasiloxane
Conditions | Yield |
---|---|
With water In tetrahydrofuran for 10h; Heating; | A n/a B n/a C n/a D 11% |
Conditions | Yield |
---|---|
(i) (hydrolysis), (ii) H2SO4, toluene; Multistep reaction; |
methylphenylsilane
A
bis(phenyl methyl hydrido)disiloxane
1,3,5-triphenyl-1,3,5-trimethylcyclotrisiloxane
C
methylphenylsiloxane
D
C14H18O2Si2
Conditions | Yield |
---|---|
With water for 2h; Ambient temperature; Further byproducts given; | A 19 % Chromat. B 32 % Chromat. C 2.3 % Chromat. D 17 % Chromat. |
1,3,5-triphenyl-1,3,5-trimethylcyclotrisiloxane
B
2,4,6,8-tetraphenyl-2,4,6,8-tetramethylcyclotetrasiloxane
C
tert-butyl alcohol
Conditions | Yield |
---|---|
In nonane at 160℃; Rate constant; Kinetics; Thermodynamic data; ΔE(excit.); |
(2-phenylpropan-2-ylperoxy)methyl(phenyl)silane
A
1-methyl-1-phenylethyl alcohol
B
bis(phenyl methyl hydrido)disiloxane
1,3,5-triphenyl-1,3,5-trimethylcyclotrisiloxane
D
poly(methylphenylsiloxane)
Conditions | Yield |
---|---|
In nonane at 160℃; Rate constant; Kinetics; Thermodynamic data; ΔE(excit.); |
dichloromethylphenylsilane
1,3,5-triphenyl-1,3,5-trimethylcyclotrisiloxane
B
cis-1,3,5-trimethyl-1,3,5-triphenylcyclorisiloxane
C
2,4,6,8-tetraphenyl-2,4,6,8-tetramethylcyclotetrasiloxane
Conditions | Yield |
---|---|
With H2O In diethyl ether; water addn. of H2O to a soln. of (CH3)(C6H5)SiCl2 in ether;; |
dichloromethylphenylsilane
1,3,5-triphenyl-1,3,5-trimethylcyclotrisiloxane
B
cis-1,3,5-trimethyl-1,3,5-triphenylcyclorisiloxane
Conditions | Yield |
---|---|
With H2O In water pouring (CH3)(C6H5)SiCl2 into icewater under vigorous stirring;; distn. at 2 torr; recrystn. from alc.;; |
d7-N,N-dimethylformamide
methylphenylsilane
1,3,5-triphenyl-1,3,5-trimethylcyclotrisiloxane
B
trimethylamine-d7
Conditions | Yield |
---|---|
With Pt(0) nanoparticles immobilized on a monolithic polymeric support at 20℃; Catalytic behavior; |
methylphenylsilane
4,4,5,5-tetramethyl-[1,3,2]-dioxaboralane
1,3,5-triphenyl-1,3,5-trimethylcyclotrisiloxane
Conditions | Yield |
---|---|
With basolite C300; water In acetonitrile at 70℃; for 7h; Inert atmosphere; |
methylphenylsilane
1,3,5-triphenyl-1,3,5-trimethylcyclotrisiloxane
B
2,4,6,8-tetraphenyl-2,4,6,8-tetramethylcyclotetrasiloxane
Conditions | Yield |
---|---|
With water; 2,3-Dihydro-1,3-diisopropyl-4,5-dimethylimidazol-2-ylidene In acetonitrile at 20℃; for 0.1h; Time; Temperature; Solvent; Schlenk technique; Glovebox; |
chloro-trimethyl-silane
2,4,6-trimethylcyclotrisiloxane
Hexamethylcyclotrisiloxane
1,3,5-triphenyl-1,3,5-trimethylcyclotrisiloxane
Conditions | Yield |
---|---|
Stage #1: 2,4,6-trimethylcyclotrisiloxane; Hexamethylcyclotrisiloxane; 1,3,5-triphenyl-1,3,5-trimethylcyclotrisiloxane With n-butyllithium In tetrahydrofuran; hexane at 70℃; Stage #2: chloro-trimethyl-silane In tetrahydrofuran; hexane | 91% |
chloro-trimethyl-silane
2,4,6-trimethylcyclotrisiloxane
Hexamethylcyclotrisiloxane
1,3,5-triphenyl-1,3,5-trimethylcyclotrisiloxane
Conditions | Yield |
---|---|
Stage #1: 2,4,6-trimethylcyclotrisiloxane; Hexamethylcyclotrisiloxane; 1,3,5-triphenyl-1,3,5-trimethylcyclotrisiloxane With n-butyllithium In tetrahydrofuran; hexane at 70℃; Stage #2: chloro-trimethyl-silane In tetrahydrofuran; hexane | 90% |
chloro-trimethyl-silane
2,4,6-trimethylcyclotrisiloxane
Hexamethylcyclotrisiloxane
1,3,5-triphenyl-1,3,5-trimethylcyclotrisiloxane
Conditions | Yield |
---|---|
Stage #1: 2,4,6-trimethylcyclotrisiloxane; Hexamethylcyclotrisiloxane; 1,3,5-triphenyl-1,3,5-trimethylcyclotrisiloxane With n-butyllithium In tetrahydrofuran; hexane at 70℃; Stage #2: chloro-trimethyl-silane In tetrahydrofuran; hexane | 88% |
chloro-trimethyl-silane
2,4,6-trimethylcyclotrisiloxane
Hexamethylcyclotrisiloxane
1,3,5-triphenyl-1,3,5-trimethylcyclotrisiloxane
Conditions | Yield |
---|---|
Stage #1: 2,4,6-trimethylcyclotrisiloxane; Hexamethylcyclotrisiloxane; 1,3,5-triphenyl-1,3,5-trimethylcyclotrisiloxane With n-butyllithium In tetrahydrofuran; hexane at 70℃; Stage #2: chloro-trimethyl-silane In tetrahydrofuran; hexane | 85% |
chloro-trimethyl-silane
2,4,6-trimethylcyclotrisiloxane
Hexamethylcyclotrisiloxane
1,3,5-triphenyl-1,3,5-trimethylcyclotrisiloxane
Conditions | Yield |
---|---|
Stage #1: 2,4,6-trimethylcyclotrisiloxane; Hexamethylcyclotrisiloxane; 1,3,5-triphenyl-1,3,5-trimethylcyclotrisiloxane With n-butyllithium In tetrahydrofuran; hexane at 70℃; Stage #2: chloro-trimethyl-silane In tetrahydrofuran; hexane | 82% |
chloro-trimethyl-silane
2,4,6-trimethylcyclotrisiloxane
Hexamethylcyclotrisiloxane
1,3,5-triphenyl-1,3,5-trimethylcyclotrisiloxane
Conditions | Yield |
---|---|
Stage #1: 2,4,6-trimethylcyclotrisiloxane; Hexamethylcyclotrisiloxane; 1,3,5-triphenyl-1,3,5-trimethylcyclotrisiloxane With n-butyllithium In tetrahydrofuran; hexane at 70℃; Stage #2: chloro-trimethyl-silane In tetrahydrofuran; hexane | 80% |
chloro-trimethyl-silane
2,4,6-trimethylcyclotrisiloxane
Hexamethylcyclotrisiloxane
1,3,5-triphenyl-1,3,5-trimethylcyclotrisiloxane
Conditions | Yield |
---|---|
Stage #1: 2,4,6-trimethylcyclotrisiloxane; Hexamethylcyclotrisiloxane; 1,3,5-triphenyl-1,3,5-trimethylcyclotrisiloxane With n-butyllithium In tetrahydrofuran; hexane at 70℃; Stage #2: chloro-trimethyl-silane In tetrahydrofuran; hexane | 80% |
chloro-trimethyl-silane
2,4,6-trimethylcyclotrisiloxane
Hexamethylcyclotrisiloxane
1,3,5-triphenyl-1,3,5-trimethylcyclotrisiloxane
Conditions | Yield |
---|---|
Stage #1: 2,4,6-trimethylcyclotrisiloxane; Hexamethylcyclotrisiloxane; 1,3,5-triphenyl-1,3,5-trimethylcyclotrisiloxane With n-butyllithium In tetrahydrofuran; hexane at 70℃; Stage #2: chloro-trimethyl-silane In tetrahydrofuran; hexane | 79% |
chloro-trimethyl-silane
2,4,6-trimethylcyclotrisiloxane
Hexamethylcyclotrisiloxane
1,3,5-triphenyl-1,3,5-trimethylcyclotrisiloxane
Conditions | Yield |
---|---|
Stage #1: 2,4,6-trimethylcyclotrisiloxane; Hexamethylcyclotrisiloxane; 1,3,5-triphenyl-1,3,5-trimethylcyclotrisiloxane With n-butyllithium In tetrahydrofuran; hexane at 70℃; Stage #2: chloro-trimethyl-silane In tetrahydrofuran; hexane | 77% |
chloro-trimethyl-silane
2,4,6-trimethylcyclotrisiloxane
Hexamethylcyclotrisiloxane
1,3,5-triphenyl-1,3,5-trimethylcyclotrisiloxane
Conditions | Yield |
---|---|
Stage #1: 2,4,6-trimethylcyclotrisiloxane; Hexamethylcyclotrisiloxane; 1,3,5-triphenyl-1,3,5-trimethylcyclotrisiloxane With n-butyllithium In tetrahydrofuran; hexane at 70℃; Stage #2: chloro-trimethyl-silane In tetrahydrofuran; hexane | 75% |
chloro-trimethyl-silane
2,4,6-trimethylcyclotrisiloxane
Hexamethylcyclotrisiloxane
1,3,5-triphenyl-1,3,5-trimethylcyclotrisiloxane
Conditions | Yield |
---|---|
Stage #1: 2,4,6-trimethylcyclotrisiloxane; Hexamethylcyclotrisiloxane; 1,3,5-triphenyl-1,3,5-trimethylcyclotrisiloxane With n-butyllithium In tetrahydrofuran; hexane at 70℃; Stage #2: chloro-trimethyl-silane In tetrahydrofuran; hexane | 74% |
chloro-trimethyl-silane
2,4,6-trimethylcyclotrisiloxane
Hexamethylcyclotrisiloxane
1,3,5-triphenyl-1,3,5-trimethylcyclotrisiloxane
Conditions | Yield |
---|---|
Stage #1: 2,4,6-trimethylcyclotrisiloxane; Hexamethylcyclotrisiloxane; 1,3,5-triphenyl-1,3,5-trimethylcyclotrisiloxane With n-butyllithium In tetrahydrofuran; hexane at 70℃; Stage #2: chloro-trimethyl-silane In tetrahydrofuran; hexane | 73% |
1,3,5-triphenyl-1,3,5-trimethylcyclotrisiloxane
chromium(0) hexacarbonyl
(CH3Si(C6H5)O)3(Cr(CO)3)3
Conditions | Yield |
---|---|
In tetrahydrofuran; dibutyl ether cyclotrisiloxane and Cr(CO)6 were dissolved in Bu2O-THF under N2, soln.was heated under reflux for 68 h; soln. was cooled, passed through a short column of Florisil/Celite, volatiles were removed under vac., residue recrystd. from benzene; | 68% |
4-Iodoacetophenone
1,3,5-triphenyl-1,3,5-trimethylcyclotrisiloxane
biphenyl-4-acetaldehyde
Conditions | Yield |
---|---|
With silver(l) oxide; tetrakis(triphenylphosphine) palladium(0) In tetrahydrofuran at 60℃; | 55% |
1,3,5-triphenyl-1,3,5-trimethylcyclotrisiloxane
A
methyldifluorophenylsilane
B
1,3-difluoro-1,3-diphenyl-1,3-dimethyldisiloxane
C
C21H24F2O2Si3
Conditions | Yield |
---|---|
With sodium tetrafluoroantimonate(III) for 0.5h; Heating; | A 45% B n/a C n/a D n/a |
para-iodoanisole
1,3,5-triphenyl-1,3,5-trimethylcyclotrisiloxane
4-methoxylbiphenyl
Conditions | Yield |
---|---|
With silver(l) oxide; tetrakis(triphenylphosphine) palladium(0) In tetrahydrofuran at 60℃; for 120h; | 39% |
1,3,5-triphenyl-1,3,5-trimethylcyclotrisiloxane
chromium(0) hexacarbonyl
A
(Si3O3(C6H5)3(CH3)3)Cr(CO)3
B
(Si3O3(C6H5)3(CH3)3){Cr(CO)3}2
Conditions | Yield |
---|---|
In n-heptane; diethylene glycol boiling mixt. of Cr(CO)6, excess ligand, diglyme and heptane for 5-6 h (Ar); Filtn., removal of solvent (vac.), chromy. on column with (silica gel, 10:1 petroleum ether-CH2Cl2), eluation of yellow zone (CH2Cl2), evapn. (vac.), sepn. of complexes by thin layer chromy. on silica gel in 2:1 C6H6/petroleum ether mixt.; elem. anal.; | A 32% B n/a |
1,3,5-triphenyl-1,3,5-trimethylcyclotrisiloxane
acetic anhydride
di(acetoxy)methyl(phenyl)silane
Conditions | Yield |
---|---|
With iron(III) chloride |
1,3,5-triphenyl-1,3,5-trimethylcyclotrisiloxane
acetic anhydride
1.3-Dimethyl-1.3-diphenyl-disiloxan-1.3-diol-diacetat
Conditions | Yield |
---|---|
With iron(III) chloride |
1,3,5-triphenyl-1,3,5-trimethylcyclotrisiloxane
acetic anhydride
1.3.5-Trimethyl-1.3.5-triphenyl-trisiloxan-1.5-diol-diacetat
Conditions | Yield |
---|---|
With iron(III) chloride |
1,3,5-triphenyl-1,3,5-trimethylcyclotrisiloxane
dimethylsilicon dichloride
1.13-Dichlor-1.1.3.5.7.9.11.13-octamethyl-3.5.7.9.11.13-hexaphenyl-heptasiloxan
Conditions | Yield |
---|---|
at 250℃; |
1,3,5-triphenyl-1,3,5-trimethylcyclotrisiloxane
dimethylsilicon dichloride
1.7-Dichlor-1.1.3.5.7-pentamethyl-3.5.7-triphenyl-tetrasiloxan
Conditions | Yield |
---|---|
at 250℃; |
The Cyclotrisiloxane,2,4,6-trimethyl-2,4,6-triphenyl-, with the CAS registry number 546-45-2, is also known as cis-2,4,6-Trimethyl-2,4,6-triphenylcyclotrisiloxane. Its EINECS registry number is 208-900-7. This chemical's molecular formula is C21H24O3Si3 and molecular weight is 408.66996. Its IUPAC name is called 2,4,6-trimethyl-2,4,6-triphenyl-1,3,5,2,4,6-trioxatrisilinane.
Physical properties of Cyclotrisiloxane,2,4,6-trimethyl-2,4,6-triphenyl-: (1)#H bond acceptors: 3; (2)#Freely Rotating Bonds: 3; (3)Index of Refraction: 1.568; (4)Molar Refractivity: 119.51 cm3; (5)Molar Volume: 365 cm3; (6)Surface Tension: 34.2 dyne/cm; (7)Density: 1.11 g/cm3; (8)Flash Point: 163.2 °C; (9)Enthalpy of Vaporization: 62.8 kJ/mol; (10)Boiling Point: 402.3 °C at 760 mmHg; (11)Vapour Pressure: 2.58E-06 mmHg at 25°C.
Uses of Cyclotrisiloxane,2,4,6-trimethyl-2,4,6-triphenyl-: it can be used to produce 1-biphenyl-4-yl-ethanone at temperature of 60 °C. This reaction will need reagent Ag2O and solvent tetrahydrofuran with reaction time of hours. The yield is about 55%.
When you are using this chemical, please be cautious about it as the following:
This chemical is harmful by inhalation, in contact with skin and if swallowed. You should avoid contacting it with skin and eyes. Whenever you will contact it, please wear suitable protective clothing, gloves and eye/face protection.
You can still convert the following datas into molecular structure:
(1)Canonical SMILES: C[Si]1(O[Si](O[Si](O1)(C)C2=CC=CC=C2)(C)C3=CC=CC=C3)C4=CC=CC=C4
(2)InChI: InChI=1S/C21H24O3Si3/c1-25(19-13-7-4-8-14-19)22-26(2,20-15-9-5-10-16-20)24-27(3,23-25)21-17-11-6-12-18-21/h4-18H,1-3H3
(3)InChIKey: HAURRGANAANPSQ-UHFFFAOYSA-N
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