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| CAS No.: | 77-63-4 |
|---|---|
| Name: | 2,4,6,8-tetramethyl-2,4,6,8-tetraphenylcyclotetrasiloxane |
| Molecular Structure: | |
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| Formula: | C28H32O4Si4 |
| Molecular Weight: | 544.902 |
| Synonyms: | 2,4,6,8-tetramethyl-2,4,6,8-tetraphenylcyclotetrasiloxane;Cyclotetrasiloxane, 2,4,6,8-tetramethyl-2,4,6,8-tetraphenyl-;2,4,6,8-Tetramethyl-2,4,6,8-tetraphenyl-1,3,5,7-tetraoxa-2,4,6,8-tetrasilacyclooctane;2,4,6,8-Tetramethyl-2,4,6,8-tetraphenylcyclooctanetetrasiloxane;2,4,6,8-Tetraphenyl-2,4,6,8-tetramethylcyclooctanetetrasiloxane;Tetrtaphenyltetramethylcyclotetrasiloxane;1,3,5,7-Tetramethyltetraphenylcyclotetrasiloxane |
| EINECS: | 201-045-0 |
| Density: | 1.13 |
| Melting Point: | 99°C |
| Boiling Point: | 493.2°C at 760 mmHg |
| Flash Point: | 211.7°C |
| PSA: | 36.92000 |
| LogP: | 3.98320 |

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% |


diethoxy-methyl-phenyl-silane


2,4,6,8-tetraphenyl-2,4,6,8-tetramethylcyclotetrasiloxane

| Conditions | Yield |
|---|---|
| With sodium hydroxide |


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.); |


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;; |


carbon dioxide


methylphenylsilane


2,4,6,8-tetraphenyl-2,4,6,8-tetramethylcyclotetrasiloxane

| Conditions | Yield |
|---|---|
| With Pt(0) nanoparticles immobilized on a monolithic polymeric support at 20℃; |

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; |

2,4,6,8-tetraphenyl-2,4,6,8-tetramethylcyclotetrasiloxane


chromium(0) hexacarbonyl


(CH3Si(C6H5)O)4(Cr(CO)3)4

| Conditions | Yield |
|---|---|
| In tetrahydrofuran; dibutyl ether cyclotetrasiloxane and Cr(CO)6 were dissolved in Bu2O-THF under N2, soln. was heated under reflux for 122 h; soln. was cooled, passed through a short column of Florisil/Celite, volatiles were removed under vac., residue recrystd. from benzene; | 79% |

2,4,6,8-tetraphenyl-2,4,6,8-tetramethylcyclotetrasiloxane


1,3-bis-(2,4-dichloro-benzoyloxymethyl)-1,1,3,3-tetramethyl-disiloxane


1,11-bis-(2,4-dichloro-benzoyloxymethyl)-1,1,3,5,7,9,11,11-octamethyl-3,5,7,9-tetraphenyl-hexasiloxane

| Conditions | Yield |
|---|---|
| With sulfuric acid |

2,4,6,8-tetraphenyl-2,4,6,8-tetramethylcyclotetrasiloxane


2-hydrido-2,4,6-trimethyl-4,6-diphenylcyclotrisiloxane

| Conditions | Yield |
|---|---|
| at 465 - 480℃; |