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396281

Sigma-Aldrich

2,4,6,8-Tetramethyl-2,4,6,8-tetravinylcyclotetrasiloxane

Synonym(s):

2,4,6,8-Tetraethenyl-2,4,6,8-tetramethylcyclotetrasiloxane

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About This Item

Linear Formula:
[-Si(CH3)(CH=CH2)O-]4
CAS Number:
Molecular Weight:
344.66
EC Number:
MDL number:
UNSPSC Code:
12162002
PubChem Substance ID:
NACRES:
NA.23

form

liquid

refractive index

n20/D 1.434 (lit.)

bp

111-112 °C/10 mmHg (lit.)

mp

−44 °C (dec.) (lit.)

density

0.997 g/mL at 25 °C (lit.)

SMILES string

C[Si]1(O[Si](C)(O[Si](C)(O[Si](C)(O1)C=C)C=C)C=C)C=C

InChI

1S/C12H24O4Si4/c1-9-17(5)13-18(6,10-2)15-20(8,12-4)16-19(7,11-3)14-17/h9-12H,1-4H2,5-8H3

InChI key

VMAWODUEPLAHOE-UHFFFAOYSA-N

General description

In the presence of a Pd catalyst, this reagent cross-couples with aryl bromides to give styrene derivatives.

Application

  • Cyclic siloxanes conjugated with fluorescent aromatic compounds as fluoride sensors: This study explores the use of cyclic siloxanes conjugated with aromatic compounds for sensing applications, offering a pathway for academic chemists interested in sensor technology and fluorescence studies (N Prigyai et al., 2020).
  • Synthesis, film morphology and performance of novel crosslinked polysiloxane with end-capped epoxy groups on cotton substrates: This article examines the chemical modification of cotton substrates using polysiloxane derivatives, which can be crucial for developing advanced textile coatings (L Hao et al., 2014).
  • Stabilizing Li-rich layered oxide cathode interface by using silicon-based electrolyte additive: This research investigates the use of a silicon-based additive derived from 2,4,6,8-tetramethyl-2,4,6,8-tetravinylcyclotetrasiloxane to enhance the stability of lithium-rich cathodes, important for chemists working with energy storage technologies (T Huang et al., 2024).

Pictograms

Health hazard

Signal Word

Danger

Hazard Statements

Hazard Classifications

Repr. 1B

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 1

Flash Point(F)

190.4 °F - closed cup

Flash Point(C)

88 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Polythiophenes are the most widely utilized semiconducting polymers in organic electronics, but they are scarcely exploited in photonics due to their high photo-induced absorption caused by interchain polaron pairs, which prevents the establishment of a window of net optical gain.
Scott E Denmark et al.
Organic letters, 8(1), 63-66 (2005-12-31)
[reaction: see text] A mild and general method for the palladium-catalyzed vinylation of aryl bromides has been developed. The use of tetrabutylammonium fluoride (TBAF) as the activator and an inexpensive and nontoxic vinyl donor, 1,3,5,7-tetramethyl-1,3,5,7-tetravinylcyclotetrasiloxane (D(4)(V), 1), allows for a
Byoung Choul Kim et al.
Small (Weinheim an der Bergstrasse, Germany), 10(19), 4020-4029 (2014-06-20)
Adjustable fluidic structures play an important role in microfluidic systems. Fracture of multilayered materials under applied tension has been previously demonstrated as a convenient, simple, and inexpensive approach to fabricate nanoscale adjustable structures; here, it is demonstrated how to extend
Mohand O Saed et al.
Scientific reports, 10(1), 6609-6609 (2020-04-22)
Liquid crystalline elastomers (LCE) undergo reversible shape changes in response to stimuli, which enables a wide range of smart applications, in soft robotics, adhesive systems or biomedical medical devices. In this study, we introduce a new dynamic covalent chemistry based on

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