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Merck
CN

226068

Sigma-Aldrich

Allyloxytrimethylsilane

98%

Synonym(s):

3-(Trimethylsiloxy)propene

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About This Item

Linear Formula:
H2C=CHCH2OSi(CH3)3
CAS Number:
Molecular Weight:
130.26
Beilstein:
1739517
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
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Assay

98%

refractive index

n20/D 1.397 (lit.)

bp

100-102 °C (lit.)

density

0.773 g/mL at 25 °C (lit.)

SMILES string

C[Si](C)(C)OCC=C

InChI

1S/C6H14OSi/c1-5-6-7-8(2,3)4/h5H,1,6H2,2-4H3

InChI key

MNMVKGDEKPPREK-UHFFFAOYSA-N

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Application

Allyloxytrimethylsilane [3-(Trimethylsiloxy)propene] was used in the synthesis of trimethylsilyl protected (3-hydroxypropyl)-trimethoxysilane.

Pictograms

FlameExclamation mark

Signal Word

Danger

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

33.8 °F - closed cup

Flash Point(C)

1 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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John B Grande et al.
Dalton transactions (Cambridge, England : 2003), 39(39), 9369-9378 (2010-08-18)
The impressive surface activity of silicones can be enhanced by the incorporation of hydrophilic organic functional groups and polymers. Traditional routes to such compounds, which typically involve platinum-catalyzed hydrosilylation, suffer from incompatibility with certain functional groups. B(C(6)F(5))(3)-catalyzed condensation of hydrosilanes
Xiuhuan Song et al.
Polymers, 11(2) (2019-04-10)
A series of hybrid thermoplastic polyurethanes (PUs) were synthesized from bi-functional polyhedral oligomeric silsesquioxane (B-POSS) and polycaprolactone (PCL) using 1,6-hexamethylene diisocyanate (HDI) as a coupling agent for the first time. The newly synthesized hybrid materials were fully characterized in terms

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