Allyltriethoxysilane, 97%, Thermo Scientific Chemicals
Allyltriethoxysilane, 97%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

Allyltriethoxysilane, 97%, Thermo Scientific Chemicals

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Quantity:
5 g
25 g
Catalog number L04297.06
also known as L04297-06
Price (USD)/ Each
50.65
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Quantity:
5 g
Request bulk or custom format
Price (USD)/ Each
50.65
Online exclusive
55.90 
Save 5.25 (9%)
Add to cart
Allyltriethoxysilane, 97%, Thermo Scientific Chemicals
Catalog numberL04297.06
Price (USD)/ Each
50.65
Online exclusive
55.90 
Save 5.25 (9%)
-
Add to cart
Chemical Identifiers
CAS2550-04-1
IUPAC Nametriethoxy(prop-2-en-1-yl)silane
Molecular FormulaC9H20O3Si
InChI KeyUMFJXASDGBJDEB-UHFFFAOYSA-N
SMILESCCO[Si](CC=C)(OCC)OCC
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SpecificationsSpecification SheetSpecification Sheet
Assay (GC)≥96.0%
Identification (FTIR)Conforms
Refractive Index1.4050-1.4105 @ 20?C
Appearance (Color)Clear colorless
FormLiquid
Allyltriethoxysilane is used as chemical additives and intermediates. It is used as general catalyst.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Allyltriethoxysilane is used as chemical additives and intermediates. It is used as general catalyst.

Solubility
Hydrolyzes in water.

Notes
Moisture Sensitive. Store away from oxidizing agents. Incompatible with moisture and oxidizing agents.
RUO – Research Use Only

General References:

  1. Shingo Yamasaki; Kunihiko Fujii; Reiko Wada; Motomu Kanai and Masakatsu Shibasaki. A General Catalytic Allylation Using Allyltrimethoxysilane.J. Am. Chem. Soc.2002, 124 (23), 6536-6537.
  2. Ying-Sing Li; Nicolas E. Vecchio; Yu Wang; Cheneel McNutt. Vibrational spectra of metals treated with allyltrimethoxysilane sol-gel and self-assembled monolayer of allytrichlorosilane..Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy.2007, 67 598-603.
  3. Phosphine-free Heck reaction with aryldiazonium fluoroborates, catalyzed by Pd(OAc)2, affords symmetrically coupled trans-stilbenes, generally in good yields; the presence of various functionalities, e.g. iodo, nitro or methoxycarbonyl, is tolerated: J. Chem. Soc., Perkin 1, 275 (1998).