3401-26-1

Usage

Uses

Used in Chemical Synthesis:
PHENYL(3-CHLOROPROPYL)DICHLOROSILANE is used as a chemical intermediate for the production of various organosilicon compounds. Its unique structure allows it to be a key component in the synthesis of these compounds, which are essential in the manufacturing of a wide range of products.
Used in Silicone Polymers Industry:
In the Silicone Polymers Industry, PHENYL(3-CHLOROPROPYL)DICHLOROSILANE is used as a precursor to create silicone polymers. These polymers are valued for their heat resistance, flexibility, and chemical stability, making them suitable for applications in various industries, including automotive, aerospace, and electronics.
Used in Sealants and Adhesives Industry:
PHENYL(3-CHLOROPROPYL)DICHLOROSILANE is used as a component in the formulation of sealants and adhesives. Its ability to form strong bonds and its resistance to environmental factors make it an ideal choice for creating durable and long-lasting sealants and adhesives.
Used in Coatings Industry:
In the Coatings Industry, PHENYL(3-CHLOROPROPYL)DICHLOROSILANE is utilized in the development of coatings with enhanced properties. Its incorporation into coating formulations contributes to improved durability, weather resistance, and overall performance.
Used as a Coupling Agent:
PHENYL(3-CHLOROPROPYL)DICHLOROSILANE is used as a coupling agent in the production of functionalized materials. Its reactive nature allows it to form strong bonds between different materials, improving their compatibility and enhancing the overall properties of the final product.
Used as a Surface Modifier:
As a surface modifier, PHENYL(3-CHLOROPROPYL)DICHLOROSILANE is employed to alter the surface properties of materials. This can lead to improved adhesion, wettability, and other surface-related characteristics, which are crucial for specific applications.
Used as a Crosslinking Agent in Silicone Rubbers:
In the preparation of silicone rubbers, PHENYL(3-CHLOROPROPYL)DICHLOROSILANE serves as a crosslinking agent. Its ability to form covalent bonds between polymer chains contributes to the development of rubbers with enhanced mechanical properties and elasticity.
Safety Precautions:
Due to its reactive nature, PHENYL(3-CHLOROPROPYL)DICHLOROSILANE must be handled and stored with extreme caution. It can react vigorously with water and other compounds, potentially producing flammable and toxic gases. Proper safety measures, including the use of protective equipment and controlled environments, are essential to prevent accidents and ensure the safe use of PHENYL(3-CHLOROPROPYL)DICHLOROSILANE.

InChI:InChI=1/C9H11Cl3Si/c10-7-4-8-13(11,12)9-5-2-1-3-6-9/h1-3,5-6H,4,7-8H2

Upstream product

• 1631-84-1 dichlorophenylsilane 
• 107-05-1 3-chloroprop-1-ene 

Downstream Products

• 74045-43-5 1-phenyl-1-vinyl-1-silacyclobutane 
• 17067-64-0 Triphenyl-(3-isocyanato-propyl)-silan 
• 162754-67-8 1-(1,2-epoxyethyl)-1-phenylsilacyclobutane 
• 138426-43-4 1-t-butoxy-1-phenyl-2-(2,2,3,3,4,4,5,5,6,6,7,7,7-tridecafluoroheptyl)silacyclopentane 
• 138426-52-5 1-acetoxy-1-phenyl-2-(2,2,3,3,4,4,5,5,6,6,7,7,7-tridecafluoroheptyl)silacyclopentane 
• 138426-39-8 1-phenyl-1-(3,3,4,4,5,5,6,6,7,7,8,8,8-trodecafluoro010iodooctyl)silacyclobutane 
• 138445-32-6 1-phenyl-1-(4,4,4-trifluoro-1-iodobutyl)silacyclobutane 
• 138426-45-6 1-t-butoxy-2-(2,2-dimethylpropyl)-1-phenylsilacyclopentane 
• 138426-49-0 1-t-butoxy-2-(2-iodoethyl)-1-phenylsilacyclopentane 
• 138426-54-7 1-acetoxy-2-(2-methylpropyl)-1-phenylsilacyclopentane 
• 138426-47-8 1-t-butoxy-2-(2-methylpropyl)-1-phenylsilacyclopentane 
• 138426-40-1 1-(1-iodo-3,3-dimethylbutyl)-1-phenylsilacyclobutane 
• 138426-42-3 1-(1,3-diiodopropyl)-1-phenylsilacyclobutane 
• 138426-41-2 1-(1-iodo-3-methylbutyl)-1-phenylsilacyclobutane 

Relevant academic research and scientific papers

Synthesis of 2-methylidene-1-silacyclohexanes from 2,6-dibromohex-1-ene and polyhalosilanes

Various 2-methylidene-1-silacyclohexanes were prepared by straightforward syntheses from readily available polychloro- or polyfluorosilanes, magnesium and 2,6-dibromohex-1-ene using Barbier-type conditions or a previously synthesized Grignard reagent. Good yields were obtained considering the low stability of the products in the reaction conditions.

Packing for use in resolution

The packing for use in resolution proposed for the liquid chromatography for particularly the opti-cal resolution of racemic compounds is prepared by reacting a silica gel carrier with a so-called silane treating agent to introduce a spacer part therein and chemically bonding it with a copper salt of a carboxylic or thiocarboxylic acid selected from the group consisting of optically active D- and L-2--acetizinecaroxylic acid, proline, hydroxyproline and allohydroxyproline. The steric bulkiness, the distance between the silica gel and the optically active group and the degree of hydrophobicity are specified so as to obtain an excellent resolving power.