Allyltriethoxysilane

Base Information

• Chemical Name: Allyltriethoxysilane
• CAS No.: 2550-04-1
• Molecular Formula: C9H20O3Si
• Molecular Weight: 204.341
• Hs Code.: 29319090
• European Community (EC) Number: 219-843-2
• NSC Number: 89735
• DSSTox Substance ID: DTXSID4062513
• Nikkaji Number: J149.315I
• Wikidata: Q72437421
• Mol file: 2550-04-1.mol

Synonyms:Allyltriethoxysilane;2550-04-1;Triethoxyallylsilane;Silane, triethoxy-2-propenyl-;triethoxy(prop-2-enyl)silane;Silane, allyltriethoxy-;Allytriethoxysilane;triethoxy(prop-2-en-1-yl)silane;NSC89735;allyl triethoxysilane;allyl-triethoxy-silane;Allyltriethoxysilane, 97%;SCHEMBL93277;CH2=CHCH2Si(OC2H5)3;DTXSID4062513;Silane, triethoxy-2-propen-1-yl-;EINECS 219-843-2;BBL103429;MFCD00009064;NSC 89735;NSC-89735;STL557239;AKOS008901194;FS-5108;A0785;FT-0634358;F17737;Allyltriethoxysilane(3-Triethoxysilyl-1-propene);J-016023

Chemical Property of Allyltriethoxysilane

Chemical Property:

• Appearance/Colour: Clear to straw liquid
• Vapor Pressure: 1.15mmHg at 25°C
• Refractive Index: n20/D 1.406(lit.)
• Boiling Point: 181.5 °C at 760 mmHg
• Flash Point: 21.1 °C
• PSA: 27.69000
• Density: 0.9 g/cm³
• LogP: 2.22080
• Storage Temp.: Flammables area
• Sensitive.: Moisture Sensitive
• Water Solubility.: Hydrolyzes in water.
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 8
• Exact Mass: 204.11817103
• Heavy Atom Count: 13
• Complexity: 122

Purity/Quality:

98% min ^*data from raw suppliers

Allyltriethoxysilane ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xi
• Hazard Codes: Xi
• Statements: 10-36/37/38-11
• Safety Statements: 26-24/25

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: CCO[Si](CC=C)(OCC)OCC
• Uses: Allyltriethoxysilane is used as chemical additives and intermediates. It is used as general catalyst.

Technology Process of Allyltriethoxysilane

There total 12 articles about Allyltriethoxysilane which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 98.0%

propene (187737-37-7,13987-01-4,15220-87-8,9003-07-0,676-63-1,25085-53-4) + Triethoxysilane (998-30-1) → propane (74-98-6) + allyltriethoxysilane (2550-04-1)

Guidance literature:

With DIP-Co catalysts; at 23 ℃; Reagent/catalyst; Inert atmosphere; Glovebox;

DOI:10.1021/acs.organomet.8b00416

Reference yield:

→ propyltriethoxysilane (2550-02-9) + allyltriethoxysilane (2550-04-1)

Guidance literature:

With C₂₈H₃₄CoN₃;

Reference yield:

tetraethoxy orthosilicate (78-10-4) + allylmagnesium bromide (2622-05-1) → allyltriethoxysilane (2550-04-1)

Guidance literature:

In diethyl ether;

upstream raw materials:

ethanol

allyltrichlorosilane

tetraethoxy orthosilicate

allyl bromide

Downstream raw materials:

allyldimethylethoxysilane

allyl-trimethyl-silane

diethoxy-allyl-phenyl-silane

3-cyanopropyl-triethoxysilane

Refernces

• 1、 Ha, Sung-Ho,Kim, Sung-Woo,Jeong, Ho-Kyun. "Investigation of reaction rate of bis(triethoxysilylpropyl)tetrasulphide in silica-filled compound using pyrolysis-gas chromatography/mass spectrometry". . p. 5245 - 5250. Retrieved 2013.
• 2、 Basu, Debashis,Gilbert-Wilson, Ryan,Gray, Danielle L.,Rauchfuss, Thomas B.,Dash, Aswini K.. "Fe and Co Complexes of Rigidly Planar Phosphino-Quinoline-Pyridine Ligands for Catalytic Hydrosilylation and Dehydrogenative Silylation". . p. 2760 - 2768. Retrieved 2018/09/10.
• 3、 -. "Dehydrogenative Silylation and Crosslinking Using Cobalt Catalysts". Paragraph 0145. . Retrieved 2014/03/24.