226068
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
EC Number:
242-031-4
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
1739517
MDL number:
InChI key
MNMVKGDEKPPREK-UHFFFAOYSA-N
InChI
1S/C6H14OSi/c1-5-6-7-8(2,3)4/h5H,1,6H2,2-4H3
SMILES string
C[Si](C)(C)OCC=C
assay
98%
bp
100-102 °C (lit.)
density
0.773 g/mL at 25 °C (lit.)
Application
Allyloxytrimethylsilane [3-(Trimethylsiloxy)propene] was used in the synthesis of trimethylsilyl protected (3-hydroxypropyl)-trimethoxysilane.
signalword
Danger
hcodes
Hazard Classifications
Eye Irrit. 2 - Flam. Liq. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
3 - Flammable liquids
wgk
WGK 3
flash_point_f
33.8 °F - closed cup
flash_point_c
1 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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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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