| Identification | More | [Name]
2,4,6,8-Tetravinyl-2,4,6,8-tetramethylcyclotetrasiloxane | [CAS]
2554-06-5 | [Synonyms]
1,3,5,7-TETRAVINYL-1,3,5,7-TETRAMETHYLCYCLOTETRASILOXANE
1,3,5,7-TETRAVINYLTETRAMETHYLCYCLOTETRASILOXANE
2,4,6,8-TETRAMETHYL-2,4,6,8-TETRAVINYLCYCLOTETRASILOXANE
2,4,6,8-TETRAMETHYLTETRAVINYLCYCLOTETRASILOXANE
2,4,6,8-Tetravinyl-2,4,6,8-tetramethylcyclotetrasiloxane
1,3,5,7-Tetramethyl-1,3,5,7-etravinylcyclotetrasiloxane
1,3,5,7-tetramethyl-1,3,5,7-tetravinylcyclotetrasiloxane
2,4,6,8-tetraethenyl-2,4,6,8-tetramethyl-cyclotetrasiloxan
2,4,6,8-tetraethenyl-2,4,6,8-tetramethylcyclotetrasiloxane
2,4,6,8-tetraethenyl-2,4,6,8-tetramethyl-Cyclotetrasiloxane
Cyclotetrasiloxane, 2,4,6,8-tetraethenyl-2,4,6,8-tetramethyl-
Cyclotetrasiloxane,2,4,6,8-tetraethenyl-2,4,6,8-tetramethyl-
s-tetramethyltetravinylcyclotetrasiloxane
Tetravinyltetramethylcyclotetrasiloxane
tetravinyl-tetramethylcyclo-tetrasiloxane
METHYLVINYLCYCLOSILOXANE
2,4,6,8-TETRAMETHYL2,4,6,8-TETRAVINYLCYCLO-TETRASILOXANE 99%
2,4,6,8-Tetravinyl-2,4,6,8-tetramethylcyclotetrasiloxane
Vinylmethylcyclosiloxane
2,4,6,8-Tetraethenyl-2,4,6,8-tetramethylcyclooctanetetrasiloxane | [EINECS(EC#)]
219-863-1 | [Molecular Formula]
C12H32O4Si4 | [MDL Number]
MFCD00040293 | [Molecular Weight]
352.72 | [MOL File]
2554-06-5.mol |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36:Irritating to the eyes. | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing . | [WGK Germany ]
1
| [RTECS ]
GZ4550000
| [F ]
10 | [TSCA ]
Yes | [HS Code ]
29319090 |
| Hazard Information | Back Directory | [Chemical Properties]
Colorless transparent liquid | [Physical properties]
bp 224–224.5 °C. | [Uses]
2,4,6,8-Tetraethenyl-2,4,6,8-tetramethylcyclotetrasiloxane (1) (D4V) and the trimer, 2,4,6-triethenyl-2,4,6- trimethylcyclotrisiloxane (2) (D3V) are the two commercially available cyclic polyvinylmethylsiloxanes. D4 V is used as a vinyl donor in the palladium-catalyzed vinylation of aryl halides and as a building block in polymer chemistry and dendrimer synthesis. The palladium-catalyzed vinylation of substituted aryl halides using D4 V is a general and mild method for the preparation of a variety of substituted styrenes or dienes.It is widely used as reagent for the vinylation of aryl halides and building block for
carbosilane dendrimers. | [General Description]
In the presence of a Pd catalyst, this reagent cross-couples with aryl bromides to give styrene derivatives. | [Hazard]
Low toxicity by ingestion and inhalation. | [Flammability and Explosibility]
Nonflammable | [Purification Methods]
A 7mL sample can be distilled in a small Vigreux column (p 11) at atmospheric pressure without polymerisation or decomposition. It is soluble in cyclohexane. [Kantor et al. J Am Chem Soc 77 1685 1955, Beilstein 4 IV 4184.] |
| Spectrum Detail | Back Directory | [Spectrum Detail]
2,4,6,8-Tetravinyl-2,4,6,8-tetramethylcyclotetrasiloxane(2554-06-5)IR
2,4,6,8-Tetravinyl-2,4,6,8-tetramethylcyclotetrasiloxane(2554-06-5)Raman
2,4,6,8-Tetravinyl-2,4,6,8-tetramethylcyclotetrasiloxane(2554-06-5)FT-IR
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| Well-known Reagent Company Product Information | Back Directory | [Alfa Aesar]
2,4,6,8-Tetramethyl-2,4,6,8-tetravinylcyclotetrasiloxane, 97%(2554-06-5) | [Sigma Aldrich]
2554-06-5(sigmaaldrich) | [TCI AMERICA]
2,4,6,8-Tetramethyl-2,4,6,8-tetravinylcyclotetrasiloxane,>97.0%(GC)(2554-06-5) |
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