Conditions | Yield |
---|---|
Stage #1: dimethylsilicon dichloride With sodium In tetrahydrofuran at 0 - 20℃; Stage #2: With naphthalene In tetrahydrofuran at 20℃; for 4h; Reagent/catalyst; Temperature; Reflux; | 87.3% |
With lithium In tetrahydrofuran at 20℃; for 0.25h; reaction in a US (ultrasonic field); | 78.4% |
With lithium In tetrahydrofuran at 20℃; for 0.25h; Product distribution; Kinetics; reaction in a US (ultrasonic) field; yield dependence on Li-surface; | 78.4% |
Conditions | Yield |
---|---|
With [pedeta*H2SiCl(+)]2*[Si6Cl14]2(-) In tetrahydrofuran at 20℃; for 24h; | 85% |
dimethylsilicon dichloride
A
decamethylcyclopentasilane
B
dodecamethylcyclohexasilane
Conditions | Yield |
---|---|
With lithium; 1,1,1-trimethyl-2,2,2-triphenyldisilane In tetrahydrofuran Yields of byproduct given; | A n/a B 80% |
dimethylsilicon dichloride
A
octamethylcyclotetrasiloxane
B
Tetradecamethylcycloheptasilan
C
decamethylcyclopentasilane
D
dodecamethylcyclohexasilane
Conditions | Yield |
---|---|
With tetrahydrofuran; lithium 0 deg C, 1 h, then 20-25 deg C, 2 h; Further byproducts given. Yields of byproduct given; | A n/a B n/a C 60% D n/a |
With tetrahydrofuran; lithium 0 deg C, 1 h, then 20-25 deg C, 2 h; Further byproducts given. Yields of byproduct given; | A n/a B n/a C n/a D 60% |
With tetrahydrofuran; lithium at -5 - 0℃; for 1h; Yield given. Further byproducts given. Yields of byproduct given; |
Methyltrichlorosilane
1,2-dichlorotetramethylsilane
A
dodecamethylcyclohexasilane
Conditions | Yield |
---|---|
With lithium In tetrahydrofuran for 3h; | A 48% B 16% C 6% D 24% |
dimethylsilicon dichloride
dichloromethylphenylsilane
A
monophenylundecamethylcyclohexasilane
B
dodecamethylcyclohexasilane
C
trans-1,4-diphenyldecamethylcyclohexasilane
Conditions | Yield |
---|---|
With potassium Sodium In tetrahydrofuran Heating; | A 24% B 8% C 1.2 g |
Conditions | Yield |
---|---|
With potassium Sodium In tetrahydrofuran |
tetradecamethylbicyclo[2.2.2]octasilane
dodecamethylcyclohexasilane
Conditions | Yield |
---|---|
In cyclohexane Irradiation; |
Tetradecamethylcycloheptasilan
dodecamethylcyclohexasilane
Conditions | Yield |
---|---|
With potassium Sodium In tetrahydrofuran at 30 - 58℃; Equilibrium constant; Thermodynamic data; ΔH, ΔS; |
1,2-dimethoxy-1,1,2,2-tetramethyldisilane
A
Tetradecamethylcycloheptasilan
B
decamethylcyclopentasilane
C
dodecamethylcyclohexasilane
Conditions | Yield |
---|---|
With sodium In tetrahydrofuran for 22h; Ambient temperature; | A n/a B n/a C 48 % Chromat. |
decamethylcyclopentasilane
dodecamethylcyclohexasilane
Conditions | Yield |
---|---|
With potassium Sodium In tetrahydrofuran at 30 - 58℃; Equilibrium constant; Thermodynamic data; ΔH, ΔS; |
tert-butyldichloromethylsilane
dimethylsilicon dichloride
A
dodecamethylcyclohexasilane
Conditions | Yield |
---|---|
With lithium In tetrahydrofuran at 0℃; Yield given; |
Di-tert-butyldichlorosilane
dimethylsilicon dichloride
A
dodecamethylcyclohexasilane
Conditions | Yield |
---|---|
With lithium In tetrahydrofuran at 0℃; |
dimethylsilicon dichloride
diphenylsilyl dichloride
A
decamethylcyclopentasilane
B
dodecamethylcyclohexasilane
Conditions | Yield |
---|---|
With lithium In tetrahydrofuran at 0℃; Yield given. Yields of byproduct given; |
dimethylsilicon dichloride
A
Hexamethylcyclotrisiloxane
B
octamethylcyclotetrasiloxane
C
decamethylcyclopentasiloxane
D
Tetradecamethylcycloheptasilan
E
decamethylcyclopentasilane
F
dodecamethylcyclohexasilane
Conditions | Yield |
---|---|
With tetrahydrofuran; lithium at 40 - 45℃; Product distribution; Mechanism; various temperature, various reactant ratios; |
dimethylsilicon dichloride
A
Tetradecamethylcycloheptasilan
B
hexadecamethylcyclooctasilane
C
decamethylcyclopentasilane
D
dodecamethylcyclohexasilane
Conditions | Yield |
---|---|
With potassium Sodium In tetrahydrofuran for 8h; Heating; Further byproducts given; | A 2.6 % Chromat. B 1.3 % Chromat. C 17 % Chromat. D 52 % Chromat. |
With potassium Sodium In tetrahydrofuran for 8h; Heating; Further byproducts given; | A 3 % Chromat. B 1.8 % Chromat. C 12 % Chromat. D 54 % Chromat. |
With lithium In tetrahydrofuran 1) 0 deg C, 6 h; 2) 20 deg C, 1 h; further conditions; Yield given. Further byproducts given; | |
With potassium Sodium In tetrahydrofuran for 8h; Heating; Further byproducts given; | A 3.0 % Chromat. B 1.8 % Chromat. C 12 % Chromat. D 54 % Chromat. |
dimethylsilicon dichloride
A
Tetradecamethylcycloheptasilan
B
1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9-Octadecamethyl-nonasilonane
C
decamethylcyclopentasilane
D
dodecamethylcyclohexasilane
Conditions | Yield |
---|---|
With potassium Sodium In tetrahydrofuran for 8h; Heating; Further byproducts given; | A 3.0 % Chromat. B 1.0 % Chromat. C 12 % Chromat. D 54 % Chromat. |
dimethylsilicon dichloride
A
Tetradecamethylcycloheptasilan
B
1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10-Icosamethyl-decasilecane
C
decamethylcyclopentasilane
D
dodecamethylcyclohexasilane
Conditions | Yield |
---|---|
With potassium Sodium In tetrahydrofuran for 8h; Heating; Further byproducts given; | A 3.0 % Chromat. B 0.23 % Chromat. C 12 % Chromat. D 54 % Chromat. |
dimethylsilicon dichloride
A
Tetradecamethylcycloheptasilan
B
1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11-Docosamethyl-1,2,3,4,5,6,7,8,9,10,11-undecasila-cycloundecane
C
decamethylcyclopentasilane
D
dodecamethylcyclohexasilane
Conditions | Yield |
---|---|
With potassium Sodium In tetrahydrofuran for 8h; Heating; Further byproducts given; | A 3.0 % Chromat. B 0.26 % Chromat. C 12 % Chromat. D 54 % Chromat. |
dimethylsilicon dichloride
A
Tetradecamethylcycloheptasilan
B
1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,12,12-Tetracosamethyl-1,2,3,4,5,6,7,8,9,10,11,12-dodecasila-cyclododecane
C
decamethylcyclopentasilane
D
dodecamethylcyclohexasilane
Conditions | Yield |
---|---|
With potassium Sodium In tetrahydrofuran for 8h; Heating; Further byproducts given; | A 3.0 % Chromat. B 0.23 % Chromat. C 12 % Chromat. D 54 % Chromat. |
dimethylsilicon dichloride
A
Tetradecamethylcycloheptasilan
B
hexacosamethylcyclotridecasilane
C
decamethylcyclopentasilane
D
dodecamethylcyclohexasilane
Conditions | Yield |
---|---|
With potassium Sodium In tetrahydrofuran for 8h; Heating; Further byproducts given; | A 3.0 % Chromat. B 0.21 % Chromat. C 12 % Chromat. D 54 % Chromat. |
dimethylsilicon dichloride
A
Tetradecamethylcycloheptasilan
B
1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,12,12,13,13,14,14-Octacosamethyl-1,2,3,4,5,6,7,8,9,10,11,12,13,14-tetradecasila-cyclotetradecane
C
decamethylcyclopentasilane
D
dodecamethylcyclohexasilane
Conditions | Yield |
---|---|
With potassium Sodium In tetrahydrofuran for 8h; Heating; Further byproducts given; | A 3.0 % Chromat. B 0.21 % Chromat. C 12 % Chromat. D 54 % Chromat. |
dimethylsilicon dichloride
A
Tetradecamethylcycloheptasilan
B
1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,12,12,13,13,14,14,15,15-Triacontamethyl-1,2,3,4,5,6,7,8,9,10,11,12,13,14,15-pentadecasila-cyclopentadecane
C
decamethylcyclopentasilane
D
dodecamethylcyclohexasilane
Conditions | Yield |
---|---|
With potassium Sodium In tetrahydrofuran for 8h; Heating; Further byproducts given; | A 3.0 % Chromat. B 0.21 % Chromat. C 12 % Chromat. D 54 % Chromat. |
dimethylsilicon dichloride
A
Tetradecamethylcycloheptasilan
B
dotriacontamethylcyclohexadecasilane
C
decamethylcyclopentasilane
D
dodecamethylcyclohexasilane
Conditions | Yield |
---|---|
With potassium Sodium In tetrahydrofuran for 8h; Heating; Further byproducts given; | A 3.0 % Chromat. B 0.18 % Chromat. C 12 % Chromat. D 54 % Chromat. |
dimethylsilicon dichloride
A
Tetradecamethylcycloheptasilan
B
1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,12,12,13,13,14,14,15,15,16,16,17,17-Tetratriacontamethyl-1,2,3,4,5,6,7,8,9,10,11,12,13,14,15,16,17-heptadecasila-cycloheptadecane
C
decamethylcyclopentasilane
D
dodecamethylcyclohexasilane
Conditions | Yield |
---|---|
With potassium Sodium In tetrahydrofuran for 8h; Heating; Further byproducts given; | A 3.0 % Chromat. B 0.13 % Chromat. C 12 % Chromat. D 54 % Chromat. |
dimethylsilicon dichloride
A
Tetradecamethylcycloheptasilan
B
1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,12,12,13,13,14,14,15,15,16,16,17,17,18,18-Hexatriacontamethyl-1,2,3,4,5,6,7,8,9,10,11,12,13,14,15,16,17,18-octadecasila-cyclooctadecane
C
decamethylcyclopentasilane
D
dodecamethylcyclohexasilane
Conditions | Yield |
---|---|
With potassium Sodium In tetrahydrofuran for 8h; Heating; Further byproducts given; | A 3.0 % Chromat. B 0.09 % Chromat. C 12 % Chromat. D 54 % Chromat. |
dimethylsilicon dichloride
A
Tetradecamethylcycloheptasilan
B
1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,12,12,13,13,14,14,15,15,16,16,17,17,18,18,19,19-Octatriacontamethyl-1,2,3,4,5,6,7,8,9,10,11,12,13,14,15,16,17,18,19-nonadecasila-cyclononadecane
C
decamethylcyclopentasilane
D
dodecamethylcyclohexasilane
Conditions | Yield |
---|---|
With potassium Sodium In tetrahydrofuran for 8h; Heating; Further byproducts given; | A 3.0 % Chromat. B 0.05 % Chromat. C 12 % Chromat. D 54 % Chromat. |
dimethylsilicon dichloride
A
Tetradecamethylcycloheptasilan
B
decamethylcyclopentasilane
C
dodecamethylcyclohexasilane
D
C48H144Si24
Conditions | Yield |
---|---|
With potassium Sodium In tetrahydrofuran for 8h; Heating; Further byproducts given; | A 3.0 % Chromat. B 12 % Chromat. C 54 % Chromat. D n/a |
dimethylsilicon dichloride
A
decamethylcyclopentasilane
B
dodecamethylcyclohexasilane
Conditions | Yield |
---|---|
With lithium; diphenylsilyl dichloride In tetrahydrofuran at 0℃; Yield given. Yields of byproduct given. Title compound not separated from byproducts; |
A
decamethylcyclopentasilane
B
dodecamethylcyclohexasilane
Conditions | Yield |
---|---|
Irradiation; |
Conditions | Yield |
---|---|
Stage #1: dodecamethylcyclohexasilane With potassium tert-butylate In tetrahydrofuran at 20℃; for 0.5h; Inert atmosphere; Schlenk technique; Stage #2: With hydrogen; C62H51N2Ni2(1-)*K(1+)*2C4H10O2 In tetrahydrofuran at 45℃; under 1500.15 Torr; for 24h; Schlenk technique; Stage #3: ethanol In tetrahydrofuran at -40 - 20℃; for 4h; Schlenk technique; | 92% |
Conditions | Yield |
---|---|
In diethyl ether at 5℃; for 1.5h; Irradiation; | 89% |
Conditions | Yield |
---|---|
In diethyl ether at 5℃; for 1.5h; Irradiation; | 87% |
Conditions | Yield |
---|---|
In diethyl ether at 5℃; for 1.5h; Irradiation; | 87% |
Conditions | Yield |
---|---|
In diethyl ether at 5℃; for 1.5h; Irradiation; | 86% |
Conditions | Yield |
---|---|
Stage #1: dimethylsilicon dichloride With sodium In tetrahydrofuran at 0 - 20℃; Stage #2: With naphthalene In tetrahydrofuran at 20℃; for 4h; Reagent/catalyst; Temperature; Reflux; | 87.3% |
With lithium In tetrahydrofuran at 20℃; for 0.25h; reaction in a US (ultrasonic field); | 78.4% |
With lithium In tetrahydrofuran at 20℃; for 0.25h; Product distribution; Kinetics; reaction in a US (ultrasonic) field; yield dependence on Li-surface; | 78.4% |
Conditions | Yield |
---|---|
With [pedeta*H2SiCl(+)]2*[Si6Cl14]2(-) In tetrahydrofuran at 20℃; for 24h; | 85% |
dimethylsilicon dichloride
A
decamethylcyclopentasilane
B
dodecamethylcyclohexasilane
Conditions | Yield |
---|---|
With lithium; 1,1,1-trimethyl-2,2,2-triphenyldisilane In tetrahydrofuran Yields of byproduct given; | A n/a B 80% |
dimethylsilicon dichloride
A
octamethylcyclotetrasiloxane
B
Tetradecamethylcycloheptasilan
C
decamethylcyclopentasilane
D
dodecamethylcyclohexasilane
Conditions | Yield |
---|---|
With tetrahydrofuran; lithium 0 deg C, 1 h, then 20-25 deg C, 2 h; Further byproducts given. Yields of byproduct given; | A n/a B n/a C 60% D n/a |
With tetrahydrofuran; lithium 0 deg C, 1 h, then 20-25 deg C, 2 h; Further byproducts given. Yields of byproduct given; | A n/a B n/a C n/a D 60% |
With tetrahydrofuran; lithium at -5 - 0℃; for 1h; Yield given. Further byproducts given. Yields of byproduct given; |
Methyltrichlorosilane
1,2-dichlorotetramethylsilane
A
dodecamethylcyclohexasilane
Conditions | Yield |
---|---|
With lithium In tetrahydrofuran for 3h; | A 48% B 16% C 6% D 24% |
dimethylsilicon dichloride
dichloromethylphenylsilane
A
monophenylundecamethylcyclohexasilane
B
dodecamethylcyclohexasilane
C
trans-1,4-diphenyldecamethylcyclohexasilane
Conditions | Yield |
---|---|
With potassium Sodium In tetrahydrofuran Heating; | A 24% B 8% C 1.2 g |
Conditions | Yield |
---|---|
With potassium Sodium In tetrahydrofuran |
tetradecamethylbicyclo[2.2.2]octasilane
dodecamethylcyclohexasilane
Conditions | Yield |
---|---|
In cyclohexane Irradiation; |
Tetradecamethylcycloheptasilan
dodecamethylcyclohexasilane
Conditions | Yield |
---|---|
With potassium Sodium In tetrahydrofuran at 30 - 58℃; Equilibrium constant; Thermodynamic data; ΔH, ΔS; |
1,2-dimethoxy-1,1,2,2-tetramethyldisilane
A
Tetradecamethylcycloheptasilan
B
decamethylcyclopentasilane
C
dodecamethylcyclohexasilane
Conditions | Yield |
---|---|
With sodium In tetrahydrofuran for 22h; Ambient temperature; | A n/a B n/a C 48 % Chromat. |
decamethylcyclopentasilane
dodecamethylcyclohexasilane
Conditions | Yield |
---|---|
With potassium Sodium In tetrahydrofuran at 30 - 58℃; Equilibrium constant; Thermodynamic data; ΔH, ΔS; |
tert-butyldichloromethylsilane
dimethylsilicon dichloride
A
dodecamethylcyclohexasilane
Conditions | Yield |
---|---|
With lithium In tetrahydrofuran at 0℃; Yield given; |
Di-tert-butyldichlorosilane
dimethylsilicon dichloride
A
dodecamethylcyclohexasilane
Conditions | Yield |
---|---|
With lithium In tetrahydrofuran at 0℃; |
dimethylsilicon dichloride
diphenylsilyl dichloride
A
decamethylcyclopentasilane
B
dodecamethylcyclohexasilane
Conditions | Yield |
---|---|
With lithium In tetrahydrofuran at 0℃; Yield given. Yields of byproduct given; |
dimethylsilicon dichloride
A
Hexamethylcyclotrisiloxane
B
octamethylcyclotetrasiloxane
C
decamethylcyclopentasiloxane
D
Tetradecamethylcycloheptasilan
E
decamethylcyclopentasilane
F
dodecamethylcyclohexasilane
Conditions | Yield |
---|---|
With tetrahydrofuran; lithium at 40 - 45℃; Product distribution; Mechanism; various temperature, various reactant ratios; |
dimethylsilicon dichloride
A
Tetradecamethylcycloheptasilan
B
hexadecamethylcyclooctasilane
C
decamethylcyclopentasilane
D
dodecamethylcyclohexasilane
Conditions | Yield |
---|---|
With potassium Sodium In tetrahydrofuran for 8h; Heating; Further byproducts given; | A 2.6 % Chromat. B 1.3 % Chromat. C 17 % Chromat. D 52 % Chromat. |
With potassium Sodium In tetrahydrofuran for 8h; Heating; Further byproducts given; | A 3 % Chromat. B 1.8 % Chromat. C 12 % Chromat. D 54 % Chromat. |
With lithium In tetrahydrofuran 1) 0 deg C, 6 h; 2) 20 deg C, 1 h; further conditions; Yield given. Further byproducts given; | |
With potassium Sodium In tetrahydrofuran for 8h; Heating; Further byproducts given; | A 3.0 % Chromat. B 1.8 % Chromat. C 12 % Chromat. D 54 % Chromat. |
dimethylsilicon dichloride
A
Tetradecamethylcycloheptasilan
B
1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9-Octadecamethyl-nonasilonane
C
decamethylcyclopentasilane
D
dodecamethylcyclohexasilane
Conditions | Yield |
---|---|
With potassium Sodium In tetrahydrofuran for 8h; Heating; Further byproducts given; | A 3.0 % Chromat. B 1.0 % Chromat. C 12 % Chromat. D 54 % Chromat. |
dimethylsilicon dichloride
A
Tetradecamethylcycloheptasilan
B
1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10-Icosamethyl-decasilecane
C
decamethylcyclopentasilane
D
dodecamethylcyclohexasilane
Conditions | Yield |
---|---|
With potassium Sodium In tetrahydrofuran for 8h; Heating; Further byproducts given; | A 3.0 % Chromat. B 0.23 % Chromat. C 12 % Chromat. D 54 % Chromat. |
dimethylsilicon dichloride
A
Tetradecamethylcycloheptasilan
B
1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11-Docosamethyl-1,2,3,4,5,6,7,8,9,10,11-undecasila-cycloundecane
C
decamethylcyclopentasilane
D
dodecamethylcyclohexasilane
Conditions | Yield |
---|---|
With potassium Sodium In tetrahydrofuran for 8h; Heating; Further byproducts given; | A 3.0 % Chromat. B 0.26 % Chromat. C 12 % Chromat. D 54 % Chromat. |
dimethylsilicon dichloride
A
Tetradecamethylcycloheptasilan
B
1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,12,12-Tetracosamethyl-1,2,3,4,5,6,7,8,9,10,11,12-dodecasila-cyclododecane
C
decamethylcyclopentasilane
D
dodecamethylcyclohexasilane
Conditions | Yield |
---|---|
With potassium Sodium In tetrahydrofuran for 8h; Heating; Further byproducts given; | A 3.0 % Chromat. B 0.23 % Chromat. C 12 % Chromat. D 54 % Chromat. |
dimethylsilicon dichloride
A
Tetradecamethylcycloheptasilan
B
hexacosamethylcyclotridecasilane
C
decamethylcyclopentasilane
D
dodecamethylcyclohexasilane
Conditions | Yield |
---|---|
With potassium Sodium In tetrahydrofuran for 8h; Heating; Further byproducts given; | A 3.0 % Chromat. B 0.21 % Chromat. C 12 % Chromat. D 54 % Chromat. |
dimethylsilicon dichloride
A
Tetradecamethylcycloheptasilan
B
1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,12,12,13,13,14,14-Octacosamethyl-1,2,3,4,5,6,7,8,9,10,11,12,13,14-tetradecasila-cyclotetradecane
C
decamethylcyclopentasilane
D
dodecamethylcyclohexasilane
Conditions | Yield |
---|---|
With potassium Sodium In tetrahydrofuran for 8h; Heating; Further byproducts given; | A 3.0 % Chromat. B 0.21 % Chromat. C 12 % Chromat. D 54 % Chromat. |
dimethylsilicon dichloride
A
Tetradecamethylcycloheptasilan
B
1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,12,12,13,13,14,14,15,15-Triacontamethyl-1,2,3,4,5,6,7,8,9,10,11,12,13,14,15-pentadecasila-cyclopentadecane
C
decamethylcyclopentasilane
D
dodecamethylcyclohexasilane
Conditions | Yield |
---|---|
With potassium Sodium In tetrahydrofuran for 8h; Heating; Further byproducts given; | A 3.0 % Chromat. B 0.21 % Chromat. C 12 % Chromat. D 54 % Chromat. |
dimethylsilicon dichloride
A
Tetradecamethylcycloheptasilan
B
dotriacontamethylcyclohexadecasilane
C
decamethylcyclopentasilane
D
dodecamethylcyclohexasilane
Conditions | Yield |
---|---|
With potassium Sodium In tetrahydrofuran for 8h; Heating; Further byproducts given; | A 3.0 % Chromat. B 0.18 % Chromat. C 12 % Chromat. D 54 % Chromat. |
dimethylsilicon dichloride
A
Tetradecamethylcycloheptasilan
B
1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,12,12,13,13,14,14,15,15,16,16,17,17-Tetratriacontamethyl-1,2,3,4,5,6,7,8,9,10,11,12,13,14,15,16,17-heptadecasila-cycloheptadecane
C
decamethylcyclopentasilane
D
dodecamethylcyclohexasilane
Conditions | Yield |
---|---|
With potassium Sodium In tetrahydrofuran for 8h; Heating; Further byproducts given; | A 3.0 % Chromat. B 0.13 % Chromat. C 12 % Chromat. D 54 % Chromat. |
The CAS register number of Dodecamethylcyclohexasilane is 4098-30-0. It also can be called as Cyclohexasilane, 1,1,2,2,3,3,4,4,5,5,6,6-dodecamethyl- and the IUPAC name about this chemical is 1,1,2,2,3,3,4,4,5,5,6,6-dodecamethylhexasilinane. The molecular formula about this chemical is C12H36Si6 and the molecular weight is 348.93. It belongs to the following product categories, such as Precursors by Metal; Vapor Deposition Precursors and so on.
Physical properties about Dodecamethylcyclohexasilane are: (1)Index of Refraction: 1.426; (2)Molar Refractivity: 108.09 cm3; (3)Molar Volume: 421.6 cm3; (4)Polarizability: 42.85x10-24cm3; (5)Surface Tension: 15.8 dyne/cm; (6)Enthalpy of Vaporization: 48.15 kJ/mol; (7)Boiling Point: 263.9 °C at 760 mmHg; (8)Vapour Pressure: 0.0163 mmHg at 25°C.
Preparation: this chemical can be prepared by dichloro-dimethyl-silane. This reaction will need reagent sodium and benzene. The reaction temperature is 200 ℃.
Uses of Dodecamethylcyclohexasilane: it can be used to produce Nonamethyl-(trimethylsilyl)-cyclopentasilan. This reaction will need reagent AlCl3 and solvent benzene.
You can still convert the following datas into molecular structure:
(1)SMILES: C[Si]1([Si]([Si]([Si]([Si](C)(C)[Si]1(C)C)(C)C)(C)C)(C)C)C
(2)InChI: InChI=1/C12H36Si6/c1-13(2)14(3,4)16(7,8)18(11,12)17(9,10)15(13,5)6/h1-12H3
(3)InChIKey: RTCLHEHPUHREBC-UHFFFAOYAE
(4)Std. InChI: InChI=1S/C12H36Si6/c1-13(2)14(3,4)16(7,8)18(11,12)17(9,10)15(13,5)6/h1-12H3
(5)Std. InChIKey: RTCLHEHPUHREBC-UHFFFAOYSA-N
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