To search by structure, left click in the box below to display the chemdraw toolbar. Then, draw the chemical structure of interest in the box using the toolbar. When your structure is complete, click “Search by Name” or “Search by SMILES” to generate the product name or SMILES respectively. This feature will search within the Gelest product database for matching chemical names or SMILES. Note: In cases where Gelest uses alternate chemical names, it may be necessary to search for the product of interest by its CAS#.
- Einecs Number 251-772-2
- HMIS 3-1-1-X
- Molecular Formula C9H15NO3Si
- Molecular Weight (g/mol) 213.31
- Purity (%) 90% contains other isomers
- TSCA No
- Boiling Point (˚C/mmHg) 110-114/0.6
- Flash Point (˚C) 180 °C
- Melting Point (˚C) 60-62°
Coupler for silica-poly(phenyleneterephthalamide) composite films.1
Together with phenyltrimethoxysilane, SIP6822.0, can be used to increase the dispersibility of mesoporous silica.2
1. Mark, J. et al. J. Mater. Chem. 1997, 7, 259.
2. Banet, P. et al. Langmuir 2008, 24, 9030.
Monoamino 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.
Arylsilane Cross-Coupling Agent
The cross-coupling reaction is a highly useful methodology for the formation of carbon-carbon bonds. It involves two reagents, with one typically being a suitable organometallic reagent - the nucleophile - and the other a suitable organic substrate, normally an unsaturated halide, tosylate or similar - the electrophile.
p-Aminophenyltrimethoxysilane; 4-(Trimethoxysilyl)aniline; 4-(Trimethoxysilyl)benzenamine
Archived, Publications & Technical Reports
Silicon Chemistry, Articles
Hatanaka and Hiyama first reported the palladium-catalyzed, fluoride-promoted reaction of aryl, alkenyl, allyl, and ethynyltrimethylsilanes with aryl, vinil and allyl halides to form the respective cross-coupled products