222058-04-0

Basic information

• Product Name: trichloro(2-ethylhexyl)silane
• Synonyms: trichloro(2-ethylhexyl)silane
• CAS NO: 222058-04-0
• Molecular Formula: C₈H₁₇Cl₃Si
• Molecular Weight: 247.66508
• Mol File: 222058-04-0.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: trichloro(2-ethylhexyl)silane(CAS DataBase Reference)
• NIST Chemistry Reference: trichloro(2-ethylhexyl)silane(222058-04-0)
• EPA Substance Registry System: trichloro(2-ethylhexyl)silane(222058-04-0)

Safety Data

• Hazardous Substances Data: 222058-04-0(Hazardous Substances Data)

Usage

Uses

Used in Plastics Industry:
Trichloro(2-ethylhexyl)silane is used as an adhesion promoter and coupling agent for the production of polyethylene, polypropylene, and other plastics. It enhances the bonding between the plastic and other materials, improving the overall strength and durability of the final product.
Used in Surface Modification:
Trichloro(2-ethylhexyl)silane is used as a surface modifier for glass, metal, and other materials. It can alter the surface properties of these materials, making them more compatible with other substances or improving their performance in specific applications.
Used in Polymer Composites:
Trichloro(2-ethylhexyl)silane is used as a surface treatment for fillers and pigments in polymer composites. This treatment can improve the dispersion and interaction of the fillers and pigments within the polymer matrix, leading to enhanced mechanical properties and performance of the composite material.

Downstream Products

• 1089687-03-5 dichloro-bis(2-ethylhexyl)silane 
• 1089687-05-7 2,6-dibromo-4,4-bis(2-ethylhexyl)-4H-silolo[3,2-b:4,5-b']dithiophene 
• 1089687-06-8 2,2′-bistrimethylstannyl-4,4′-bis-(2-ethylhexyl)dithieno[3,2-b:2′,3′-d]silole 

Relevant articles and documents

FUSED RING DERIVATIVE AND ORGANIC SOLAR CELL COMPRISING THE SAME

The present invention relates to a condensed cyclic derivative represented by chemical formula 1, and an organic solar cell containing the same. According to an embodiment of the present invention, the condensed cyclic derivative exhibits excellent coating properties by having a hydroxyl group, an alkyl group, an alkoxy group, and a sulfide group as a substituent.COPYRIGHT KIPO 2017

CONJUGATED POLYMERS FOR ELECTRONIC DEVICES

A conjugated polymer for electronic devices can include a repeated unit having the structure of formula (I)

Synthesis, characterization, and photovoltaic properties of a low band gap polymer based on silole-containing polythiophenes and 2,1,3-benzothiadiazole

A new low band gap silole-containing conjugated polymer, PSBTBT, was designed and synthesized. Photovoltaic properties of PSBTBT were initially investigated, and an average power conversion efficiency (PCE) of 4.7 % with a best PCE of 5.1 % was recorded under illumination (AM 1.5G, 100 mW/cm2). The response range of the device covers the whole visible range from 380 to 800 nm. These results indicate that PSBTBT is a promising polymer material for applications in polymer solar cells. Copyright