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998-30-1 - Triethoxysilane, 96% - B22063 - Alfa Aesar

B22063 Triethoxysilane, 96%

Número CAS
998-30-1
Nombre Alternativo

Tamaño Precio ($) Cantidad Disponibilidad
10g 37,50
50g 104,00
250g 414,00
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Triethoxysilane, 96%

MDL
MFCD00009061
EINECS
213-650-7

Propiedades químicas

Fórmula
C6H16O3Si
Peso molecular
164.28
Punto de fusión
-170°
Punto de ebullición
134-135°
Punto de inflamabilidad
26°(78°F)
Densidad
0.885
Índice de refracción
1.3770
Sensibilidad
Moisture Sensitive
Solubilidad
Insoluble in water. Soluble in organic solvents.

Aplicaciones

Triethoxysilane is raw material for synthesis of silane addition agent and silicon oil. It is used as a reducing agent.

Notas

Moisture sensitive. Store away from strong oxidizing agents, strong acids, bases, water/ moisture. Store under inert gas.

Referencias documentales

Miki Murata; Masanori Ishikura; Masayuki Nagata; Shinji Watanabe; and Yuzuru Masuda. Rhodium(I)-Catalyzed Silylation of Aryl Halides with Triethoxysilane:? Practical Synthetic Route to Aryltriethoxysilanes. Org. Lett. 2002, 4 (11), 1843-1845.

Amy S. Manoso and Philip DeShong. Improved Synthesis of Aryltriethoxysilanes via Palladium(0)-Catalyzed Silylation of Aryl Iodides and Bromides with Triethoxysilane. J. Org. Chem. 2001, 66 (22), 7449-7455.

In the presence of KF or CsF, reduces aldehydes and ketones to alcohols (via the silyl ether): Tetrahedron, 37, 2165 (1981). With CsF, enones can be reduced selectively to allylic alcohols in high yield: Tetrahedron., 39, 999 (1983).

Versatile hydrosilylating agent. For use in combination with Ti(O-i-Pr) 4 in a catalytic system for reduction of esters to alcohols, see: J. Org. Chem ., 57, 3751 (1992). CAUTION! Highly pyrophoric SiH 4 can form in this reaction: J. Org. Chem., 57, 3221 (1993).

The same system effects the otherwise difficult reduction of phosphine oxides to phosphines. The products may be reacted in situ with alkyl halides to give a convenient one-pot conversion of phosphine oxides to phosphonium salts: Tetrahedron Lett., 35, 625 (1994).

Pd(0)-catalyzed silylation of aryl iodides provides a route to aryl triethoxysilanes: J. Org. Chem., 62, 8569 (1997).

Indicaciones de peligro y de precaución del GHS

Indicaciones de peligro (UE): H226-H330-H314-H318

Flammable liquid and vapour. Fatal if inhaled. Causes severe skin burns and eye damage. Causes serious eye damage.

Indicaciones de precaución: P303+P361+P353-P304+P340-P305+P351+P338-P320-P405-P501a

IF ON SKIN (or hair): Remove/Take off immediately all contaminated clothing. Rinse skin with water/shower. IF INHALED: Remove to fresh air and keep at rest in a position comfortable for breathing. IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. Specific treatment is urgent (see label). Store locked up. Dispose of contents/container in accordance with local/regional/national/international regulations.

Otras referencias

Beilstein
1738989
Clase de peligro
6.1
Grupo de embalaje
I
Código de tarifa arancelaria unificado
2920.90
TSCA
Yes
RTECS
VV6682000

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