2549-99-7

Basic information

• Product Name: BENZYLTRIETHOXYSILANE
• Synonyms: Silane, triethoxy(phenylmethyl)-;triethoxy(phenylmethyl)-silan;triethoxy(phenylmethyl)-Silane;BENZYLTRIETHOXYSILANE;TRIETHOXY-BENZYL-SILANE
• CAS NO: 2549-99-7
• Molecular Formula: C₁₃H₂₂O₃Si
• Molecular Weight: 254.4
• EINECS: 219-841-1
• Product Categories: Si (Classes of Silicon Compounds);Si-O Compounds;Trialkoxysilanes
• Mol File: 2549-99-7.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 148 °C
• Flash Point: 127°C
• Appearance: /
• Density: 0.986
• Vapor Pressure: 0.0402mmHg at 25°C
• Refractive Index: 1.4628
• CAS DataBase Reference: BENZYLTRIETHOXYSILANE(CAS DataBase Reference)
• NIST Chemistry Reference: BENZYLTRIETHOXYSILANE(2549-99-7)
• EPA Substance Registry System: BENZYLTRIETHOXYSILANE(2549-99-7)

Safety Data

• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• TSCA: Yes
• Hazardous Substances Data: 2549-99-7(Hazardous Substances Data)

Usage

General Description

Benzyltriethoxysilane is a chemical compound containing a benzyl group and three ethoxy groups bonded to a central silicon atom. It is commonly used as a silane coupling agent in the production of advanced materials such as adhesives, coatings, and sealants. Benzyltriethoxysilane can improve the adhesion and durability of these materials by promoting bonding between organic and inorganic components. It is also used as a precursor in the synthesis of silicon-containing polymers and used in the modification of surfaces to enhance their properties. Additionally, benzyltriethoxysilane can act as a crosslinking agent in the formation of silicone rubbers and resins. Overall, it is a versatile chemical with various applications in the production of advanced materials.

InChI:InChI=1/C13H22O3Si/c1-4-14-17(15-5-2,16-6-3)12-13-10-8-7-9-11-13/h7-11H,4-6,12H2,1-3H3

Upstream product

• 998-30-1 Triethoxysilane 
• 108-88-3 toluene 
• 770-10-5 benzyltrichlorosilane 
• 64-17-5 ethanol 

Downstream Products

• 108-88-3 toluene 
• 140-29-4 phenylacetonitrile 
• 4980-70-5 1,3-diphenyl-1-propyne 
• 101-81-5 Diphenylmethane 
• 102261-92-7 1-benzyloxy-2,2,6,6-tetramethylpiperidine 
• 23450-31-9 4-benzylbenzonitrile 
• 27356-87-2 ethyl 2-phenethylpropenoate 
• 100-47-0 benzonitrile 
• 75553-23-0 (E)-5-phenyl-2-penten-1-ol 
• 39520-63-3 (Z)-5-phenylpent-2-en-1-ol 

Relevant articles and documents

STABILIZATION OF ACTIVE METAL CATALYSTS AT METAL-ORGANIC FRAMEWORK NODES FOR HIGHLY EFFICIENT ORGANIC TRANSFORMATIONS

Metal-organic framework (MOFs) compositions based on post?synthetic metalation of secondary building unit (SBU) terminal or bridging OH or OH2 groups with metal precursors or other post-synthetic manipulations are described. The MOFs provide a versatile family of recyclable and reusable single-site solid catalysts for catalyzing a variety of asymmetric organic transformations, including the regioselective boryiation and siiylation of benzyiic C—H bonds, the hydrogenation of aikenes, imines, carbonyls, nitroarenes, and heterocycles, hydroboration, hydrophosphination, and cyclization reactions. The solid catalysts can also be integrated into a flow reactor or a supercritical fluid reactor.

Preparation of organically modified silicon dioxides

Process for the preparation of modified, porous silicon dioxides by the hydrolytic polycondensation of tetraalkoxysilanes or polyalkoxysiloxanes in the heterogenous phase in the presence of an organoalkoxysilane.