18407-48-2

Basic information

• Product Name: Silane, methoxymethyldiphenyl-
• CAS NO: 18407-48-2
• Molecular Formula: C14H16OSi
• Molecular Weight: 228.366
• Mol File: 18407-48-2.mol
• Article Data: 17

Chemical Properties

• CAS DataBase Reference: Silane, methoxymethyldiphenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Silane, methoxymethyldiphenyl-(18407-48-2)
• EPA Substance Registry System: Silane, methoxymethyldiphenyl-(18407-48-2)

Safety Data

• Hazardous Substances Data: 18407-48-2(Hazardous Substances Data)

Usage

General Description

Silane, methoxymethyldiphenyl- is a compound used in the production of silicone polymers and resins. It is a type of silane coupling agent, which is a molecule that is used to improve the bond between inorganic materials and organic polymers. Silane, methoxymethyldiphenyl- is particularly useful for enhancing adhesion and durability in silicone-based coatings, sealants, and adhesives. It reacts with hydroxyl groups on surfaces such as glass, metal, or ceramics, forming a strong chemical bond that improves the performance of the silicone material. Overall, silane, methoxymethyldiphenyl- plays a crucial role in the formulation of high-performance silicone products used in various industrial and consumer applications.

Upstream product

• 287978-57-8 diphenylmethylsilyl formate 
• 67-56-1 methanol 
• 776-76-1 methyldiphenylsilane 
• 98-95-3 nitrobenzene 
• 1185-55-3 Methyltrimethoxysilan 
• 100-59-4 phenylmagnesium chloride 
• 1172-76-5 1,2-dimethyl-1,1,2,2-tetraphenyldisilane 
• 6843-66-9 dimethoxy(diphenyl)silane 
• 75-16-1 methylmagnesium bromide 
• 3944-09-0 1,1-diphenylsilacyclobutane 
• 18080-94-9 1,1-diphenylsilene 
• 76889-05-9 1,1,3-Triphenyl-1-silacyclobutan 
• 144-79-6 chloromethyldiphenylsilane 

Downstream Products

• 17739-53-6 di-phenylmethylsilyl fluoride 
• 807-28-3 1,3-Dimethyl-1,1,3,3-tetraphenyldisiloxan 
• 776-76-1 methyldiphenylsilane 
• 1450-16-4 1,1,1,2-tetramethyl-2,2-diphenyldisilane 
• 6231-82-9 -methanol 

Relevant articles and documents

THERMOLYSE UND PHOTOLYSE EINIGER SILA- UND DISILACYCLOBUTANE

The thermolysis of some 1,1-di- or 1,1,2-tri-substituted 1-silacyclobutanes leads to 1,3-disilacyclobutanes or to polymeric products.A possible intermediate silaalkene could not be stabilized, even in the presence of bulky substituents at the silicon atom.Photolysis of some di- or tri-substituted silacyclobutanes in methanol results in ring opening or in elimination of an alkene with further reaction of the intermediates with the solvent.Photolysis of the 1,1-diphenyl-2-methyl-1-silacyclobutane in cyclohexane leads to the 1,1,3,3-tetraphenyl-1,3-disilacyclobutane.The influence of the substituents at the silicon or the carbon atom on the reaction pathways is discussed.Photolysis opening and addition of methanol, whereas the 1,1,3,3-tetraphenyl-1,3-disilacyclobutane does not show any reaction.

Highly Selective Hydroxylation and Alkoxylation of Silanes: One-Pot Silane Oxidation and Reduction of Aldehydes/Ketones

An efficient chemoselective iridium-catalyzed method for the hydroxylation and alkoxylation of organosilanes to generate hydrogen gas and silanols or silyl ethers was developed. A variety of sterically hindered silanes with alkyl, aryl, and ether groups were tolerated. Furthermore, this atom-economical catalytic protocol can be used for the synthesis of silanediols and silanetriols. A one-pot silane oxidation and chemoselective reduction of aldehydes/ketones was also realized.

Synthesis of phenyl-methyl dialkoxy silane method of the

The invention relates to a method for synthesizing phenyl methyl dialkoxyl silane with high selectivity. The structural formula of phenyl methyl dialkoxyl silane is PhMeSi(OR)2, in which R is alkyl with 1-6 carbons. The method is characterized by comprising the following steps of: performing reaction with methyl trialkoxyl silane based on non-cyclic ether compounds such as ethyl ether as a reaction liquor and a bromobenzene Grignard reagent as a raw material; and then, obtaining the target compound, i.e., phenyl methyl dialkoxyl silane with high selectivity and high yield through simple filtering and fractional purification, and meanwhile, greatly inhibiting the generation of a byproduct diphenyl methyl alkoxyl silane.