Gelest, Inc. (3-CYCLOPENTADIENYLPROPYL)TRIETHOXYSILANE SIC2520.0

Description
Additional Properties Hydrolytic Sensitivity 7: reacts slowly with moisture/water Application Employed in silica-supported purification of fullerenes.1 Reference 1. Nie, B. et al. J. Org. Chem. 1996, 61, 1870. Safety Packaging Under Nitrogen Olefin Functional Trialkoxy Silane Silane coupling agents have the ability to form a durable bond between organic and inorganic materials to generate desired heterogeneous environments or to incorporate the bulk properties of different phases into a uniform composite structure. The general formula has two classes of functionality. The hydrolyzable group forms stable condensation products with siliceous surfaces and other oxides such as those of aluminum, zirconium, tin, titanium, and nickel. The organofunctional group alters the wetting or adhesion characteristics of the substrate, utilizes the substrate to catalyze chemical transformations at the heterogeneous interface, orders the interfacial region, or modifies its partition characteristics, and significantly effects the covalent bond between organic and inorganic materials. (3-Cyclopentadienylp ropyl)triethoxysilan e; 3-(Triethoxysilyl)pr opyl-3-cyclopentadie ne Can form dimer which may be cracked to monomer at ~190 °C at 100 mmHg Used in microparticle surface modification Employed in silica-supported purification of fullerenes
Description
Additional Properties Hydrolytic Sensitivity 7: reacts slowly with moisture/water Application Employed in silica-supported purification of fullerenes.1 Reference 1. Nie, B. et al. J. Org. Chem. 1996, 61, 1870. Safety Packaging Under Nitrogen Olefin Functional Trialkoxy Silane Silane coupling agents have the ability to form a durable bond between organic and inorganic materials to generate desired heterogeneous environments or to incorporate the bulk properties of different phases into a uniform composite structure. The general formula has two classes of functionality. The hydrolyzable group forms stable condensation products with siliceous surfaces and other oxides such as those of aluminum, zirconium, tin, titanium, and nickel. The organofunctional group alters the wetting or adhesion characteristics of the substrate, utilizes the substrate to catalyze chemical transformations at the heterogeneous interface, orders the interfacial region, or modifies its partition characteristics, and significantly effects the covalent bond between organic and inorganic materials. (3-Cyclopentadienylp ropyl)triethoxysilan e; 3-(Triethoxysilyl)pr opyl-3-cyclopentadie ne Can form dimer which may be cracked to monomer at ~190 °C at 100 mmHg Used in microparticle surface modification Employed in silica-supported purification of fullerenes

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Product
Description
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(3-CYCLOPENTADIENYLPROPYL)TRIETHOXYSILANE - SIC2520.0 - Gelest, Inc.
Morrisville, PA, United States
(3-CYCLOPENTADIENYLPROPYL)TRIETHOXYSILANE
SIC2520.0
(3-CYCLOPENTADIENYLPROPYL)TRIETHOXYSILANE SIC2520.0
Additional Properties Hydrolytic Sensitivity 7: reacts slowly with moisture/water Application Employed in silica-supported purification of fullerenes.1 Reference 1. Nie, B. et al. J. Org. Chem. 1996, 61, 1870. Safety Packaging Under Nitrogen Olefin Functional Trialkoxy Silane Silane coupling agents have the ability to form a durable bond between organic and inorganic materials to generate desired heterogeneous environments or to incorporate the bulk properties of different phases into a uniform composite structure. The general formula has two classes of functionality. The hydrolyzable group forms stable condensation products with siliceous surfaces and other oxides such as those of aluminum, zirconium, tin, titanium, and nickel. The organofunctional group alters the wetting or adhesion characteristics of the substrate, utilizes the substrate to catalyze chemical transformations at the heterogeneous interface, orders the interfacial region, or modifies its partition characteristics, and significantly effects the covalent bond between organic and inorganic materials. (3-Cyclopentadienylp ropyl)triethoxysilan e; 3-(Triethoxysilyl)pr opyl-3-cyclopentadie ne Can form dimer which may be cracked to monomer at ~190 °C at 100 mmHg Used in microparticle surface modification Employed in silica-supported purification of fullerenes

Additional Properties


  • Hydrolytic Sensitivity 7: reacts slowly with moisture/water
    Application
    Employed in silica-supported purification of fullerenes.1
    Reference
    1. Nie, B. et al. J. Org. Chem. 1996, 61, 1870.
    Safety
  • Packaging Under Nitrogen
    Olefin Functional Trialkoxy Silane
    Silane coupling agents have the ability to form a durable bond between organic and inorganic materials to generate desired heterogeneous environments or to incorporate the bulk properties of different phases into a uniform composite structure. The general formula has two classes of functionality. The hydrolyzable group forms stable condensation products with siliceous surfaces and other oxides such as those of aluminum, zirconium, tin, titanium, and nickel. The organofunctional group alters the wetting or adhesion characteristics of the substrate, utilizes the substrate to catalyze chemical transformations at the heterogeneous interface, orders the interfacial region, or modifies its partition characteristics, and significantly effects the covalent bond between organic and inorganic materials.
    (3-Cyclopentadienylpropyl)triethoxysilane; 3-(Triethoxysilyl)propyl-3-cyclopentadiene
  • Can form dimer which may be cracked to monomer at ~190 °C at 100 mmHg
  • Used in microparticle surface modification
  • Employed in silica-supported purification of fullerenes
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Technical Specifications

  Gelest, Inc.
Product Category Inorganic Chemicals and Compounds
Product Number SIC2520.0
Product Name (3-CYCLOPENTADIENYLPROPYL)TRIETHOXYSILANE
Chemical Formula C 1 4 H 2 6 O 3 Si
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