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2-[2-(TRICHLOROSILYL)ETHYL]PYRIDINE is an organosilicon compound characterized by the presence of a pyridine ring and a trichlorosilyl group attached to an ethyl chain. 2-[2-(TRICHLOROSILYL)ETHYL]PYRIDINE is known for its solubility in organic solvents and its ability to form strong covalent bonds with surfaces and other molecules, which makes it a versatile reagent for surface functionalization and a valuable precursor in the synthesis of various organosilicon compounds.

17082-69-8

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17082-69-8 Usage

Uses

Used in Surface Functionalization:
2-[2-(TRICHLOROSILYL)ETHYL]PYRIDINE is used as a reagent for surface functionalization due to its trichlorosilyl group, which facilitates the formation of strong covalent bonds with surfaces, enabling the modification of materials for specific purposes.
Used in Synthesis of Organosilicon Compounds:
In the chemical industry, 2-[2-(TRICHLOROSILYL)ETHYL]PYRIDINE serves as a precursor in the synthesis of a variety of organosilicon compounds, contributing to the development of new materials with tailored properties.
Used in Coatings Industry:
2-[2-(TRICHLOROSILYL)ETHYL]PYRIDINE is used as a component in the development of coatings, where its ability to bond with surfaces enhances the adhesion and performance of the coating materials.
Used in Adhesives Industry:
2-[2-(TRICHLOROSILYL)ETHYL]PYRIDINE is also utilized in the formulation of adhesives, improving their bonding strength and durability through its reactive trichlorosilyl group.
Used in Electronics Industry:
2-[2-(TRICHLOROSILYL)ETHYL]PYRIDINE finds application in the electronics sector, where it may be employed in the creation of materials for semiconductors, sensors, or other electronic components that require specific surface properties or chemical functionalities.

Check Digit Verification of cas no

The CAS Registry Mumber 17082-69-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,0,8 and 2 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 17082-69:
(7*1)+(6*7)+(5*0)+(4*8)+(3*2)+(2*6)+(1*9)=108
108 % 10 = 8
So 17082-69-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H8Cl3NSi/c8-12(9,10)6-4-7-3-1-2-5-11-7/h1-3,5H,4,6H2

17082-69-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name trichloro(2-pyridin-2-ylethyl)silane

1.2 Other means of identification

Product number -
Other names Trichlor-(2-[2]pyridyl-aethyl)-silan

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:17082-69-8 SDS

17082-69-8Relevant academic research and scientific papers

Tailoring photoluminescence properties in ionic nanoparticle networks

Kronstein, Martin,Akbarzadeh, Johanna,Drechsel, Christina,Peterlik, Herwig,Neouze, Marie-Alexandra

, p. 10763 - 10774 (2014/12/10)

To investigate the original and promising luminescence properties of ionic nanoparticle networks (INN), various material compositions were investigated. In this work, the linker used to network the silica nanoparticles was varied; numerous substituted or non-substituted imidazolium, pyrazolium and pyridinium linkers are presented. Photoluminescence experiments on the INN hybrid materials revealed strong emission bands over a broad range in the visible region of the light spectrum. Varying the aromatic linker between the imidazolium units induced clear shifts of the emission maxima up to 100 nm, as a consequence of π-π stacking interactions. Steric hindrance and inductive effects of the substituents, introduced on the aromatic units, also strongly influenced the luminescence properties of the materials by modifying the π-π stacking between the imidazolium rings. Small and wide-angle X-ray scattering (SAXS, WAXS) experiments revealed a clear trend between the obtained structural parameters (short-range order parameter and distance of the aromatic units within the hybrid material) and the luminescence quantum yields of the INN materials. Inducing luminescence: Interesting luminescence properties were observed in ionic nanoparticle networks containing no luminophore. "Playing" with the nanoparticle linker allowed tailoring of the excitation and emission wavelength over a broad range. A clear trend between the obtained structural parameters (obtained from small-angle X-ray scattering experiments) and the luminescence quantum yields of the ionic nanoparticle network materials could be evidenced (see figure).

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