3439-97-2

Usage

Uses

Used in Adhesives and Sealants Industry:
Silane, methyltriphenoxy(6CI,7CI,8CI,9CI) is used as a coupling agent and adhesion promoter for enhancing the bonding between different materials, such as polymers and inorganic substrates. It helps in forming a strong interface, which improves the performance and durability of adhesives and sealants.
Used in Coatings Industry:
In the coatings industry, Silane, methyltriphenoxy(6CI,7CI,8CI,9CI) is utilized as a coupling agent to improve the adhesion of coatings to various substrates. This results in better durability and performance of the coatings, making them suitable for various applications, such as automotive and construction.
Used in Construction Industry:
Silane, methyltriphenoxy(6CI,7CI,8CI,9CI) is used in the construction industry to enhance the surface properties of materials, such as water repellency and corrosion resistance. This improves the overall performance and longevity of construction materials, contributing to more durable and reliable structures.
Used in Automotive Industry:
In the automotive industry, Silane, methyltriphenoxy(6CI,7CI,8CI,9CI) is employed as a coupling agent to improve the bonding between different materials used in vehicle components. This enhances the durability and performance of automotive parts, ensuring their reliability and longevity.
Used in Electronics Industry:
Silane, methyltriphenoxy(6CI,7CI,8CI,9CI) is also used in the electronics industry to improve the adhesion and bonding of various materials, such as polymers and inorganic substrates, in electronic components. This contributes to the enhanced performance and durability of electronic devices and components.

InChI:InChI=1/C19H18O3Si/c1-23(20-17-11-5-2-6-12-17,21-18-13-7-3-8-14-18)22-19-15-9-4-10-16-19/h2-16H,1H3

Upstream product

• 75-79-6 Methyltrichlorosilane 
• 108-95-2 phenol 
• 18551-79-6 bis-[(diethoxy-methyl-silanyl)-methyl]-methyl-amine 
• 946-80-5 (benzyloxy)benzene 

Downstream Products

• 6026-29-5 -diphenyl-amin 
• 6026-26-2 Butylamino-diphenoxy-methyl-silan 

Relevant academic research and scientific papers

METHOD OF PRODUCING A HYDROLYZABLE SILICON-CONTAINING COMPOUND

The present invention provides a safe, inexpensive, and high yield means of producing a hydrolyzable silicon-containing compound, e.g., an organooxysilane and the like. A compound (A) represented by the general formula R1-O-R2 wherein R1 represents a C4-30, substituted or unsubstituted, tertiary alkyl group or aralkyl group and R2 represents a C1-30, substituted or unsubstituted, monovalent hydrocarbyl group or acyl group, is reacted in the presence of a Lewis acid catalyst with a halosilane (B) represented by the general formula R3mSiX4-m wherein R3 represents the hydrogen atom or a C1-30 substituted or unsubstituted monovalent hydrocarbyl group, X is independently bromine or chlorine, and m represents an integer from 0 to 3.

Practical conversion of chlorosilanes into alkoxysilanes without generating HCl

Alcohol-free: A versatile, efficient, and practical synthesis of alkoxysilanes without generation of HCl involves the reaction of chlorosilanes with unsymmetrical ethers in the presence of a Lewis acid (see scheme). The reaction proceeds through selective cleavage of C-O bonds and is superior to conventional processes. Industrially feasible reagents are used and only one by-product results. Copyright

N,N-Bis[ethoxy(methyl)silylmethyl]methylamines MeN[CH2SiMem(OEt)3-m]2 (m = 0 - 2). Synthesis and reactions with phenol

Previously unknown N,N-bis[ethoxy(methyl)silylmethyl]amines MeN[CH2SiMem(OEt)3-m]2 (m = 0-2) were synthesized. According to UV spectral data, only MeN[CH2SiMe2(OEt)]2 form hydrogen bond with phenol in a heptane solution. The amines with m = 0 and 1 fail to forms hydrogen bond with phenol [under the same conditions, N-(triethoxysilylmethyl)dimethylamine Me2NCH2Si(OEt)3 forms a strong hydrogen bond with phenol]. All the amines (m = 0 - 2) enter transetherification with phenol to give compounds of the general formula MeN[CH2SiMem(OPh)n(OEt)3-m-n]2 (m = 0 - 2, n = 1 - 3). Refluxing of N,N-bis[ethoxy(methyl) silylmethyl]amines with excess phenol results in cleavage of the Si-C bond by phenol, providing phenoxysilanes MemSi(OPh)4-m (m = 0 - 2) and trimethylamine.