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

Allyltriethoxysilane, 97%

CAS: 2550-04-1 | C9H20O3Si | 204.34 g/mol
製品番号(カタログ番号) L04297.06
または、製品番号L04297-06
価格(JPY)
-
数量:
5 g
一括またはカスタム形式をリクエストする
化学物質識別子
CAS2550-04-1
IUPAC Nametriethoxy(prop-2-en-1-yl)silane
Molecular FormulaC9H20O3Si
InChI KeyUMFJXASDGBJDEB-UHFFFAOYSA-N
SMILESCCO[Si](CC=C)(OCC)OCC
さらに表示
Assay (GC)≥94.0%
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).