17964-10-2

Basic information

• Product Name: DIETHYLDIPHENYLSILANE
• Synonyms: diethyldiphenyl-silan;DIPHENYLDIETHYLSILANE;DIETHYLDIPHENYLSILANE;Diethyldiphenylsilane(Diphenyldiethylsilane);Silane,diethyldiphenyl-
• CAS NO: 17964-10-2
• Molecular Formula: C₁₆H₂₀Si
• Molecular Weight: 240.42
• Mol File: 17964-10-2.mol

Chemical Properties

• Boiling Point: 144 °C
• Flash Point: 122°C
• Appearance: /
• Density: 0.95g/cm³
• Vapor Pressure: 0.00189mmHg at 25°C
• Refractive Index: 1.538
• CAS DataBase Reference: DIETHYLDIPHENYLSILANE(CAS DataBase Reference)
• NIST Chemistry Reference: DIETHYLDIPHENYLSILANE(17964-10-2)
• EPA Substance Registry System: DIETHYLDIPHENYLSILANE(17964-10-2)

Safety Data

• Hazardous Substances Data: 17964-10-2(Hazardous Substances Data)

Usage

Uses

Used in Organic Synthesis:
Diethyldiphenylsilane is used as a coupling reagent in organic synthesis for the formation of carbon-silicon bonds, which are crucial in creating organosilicon compounds with specific properties and applications.
Used in the Production of Organosilicon Compounds:
As a precursor, diethyldiphenylsilane is utilized in the synthesis of a variety of organosilicon compounds, which have applications in materials science, pharmaceuticals, and other industries due to their unique properties.
Used in Reducing Agents for Organic Reactions:
Diethyldiphenylsilane serves as a reducing agent in certain organic reactions, facilitating specific transformations that are not easily achieved with other reagents.
Used in the Production of High-Temperature Silicon Carbides:
In the manufacturing process of high-temperature silicon carbides, which are essential for applications requiring materials with extreme heat resistance, diethyldiphenylsilane is used as a source of silicon.

InChI:InChI=1/C16H20Si/c1-3-17(4-2,15-11-7-5-8-12-15)16-13-9-6-10-14-16/h5-14H,3-4H2,1-2H3

Upstream product

• 591-51-5 phenyllithium 
• 1719-53-5 diethyldichlorosilane 
• 925-90-6 ethylmagnesium bromide 
• 80-10-4 diphenylsilyl dichloride 
• 2987-77-1 triethylphenylsilane 
• 557-20-0 diethylzinc 
• 98-13-5 Phenyltrichlorosilane 
• 18666-24-5 ethyltriphenylsilane 
• 76-86-8 Triphenylsilyl chloride 
• 6990-64-3 triphenylsilyl bromide 
• 591-50-4 iodobenzene 
• 542-91-6 H₂SiEt₂ 

Downstream Products

• 17933-80-1 diethyl-bis-(3-nitro-phenyl)-silane 
• 18673-67-1 bis-(3-acetylamino-phenyl)-diethyl-silane 
• 17937-96-1 diethyl-bis-(3-amino-phenyl)-silane 

Relevant articles and documents

Integrated palladium-catalyzed arylation of heavier groupa 14 hydrides

A convenient procedure has been developed for the preparation of Groupa 14 compounds by integrated palladium-catalyzed cross-coupling of aromatic iodides with the corresponding Groupa 14 hydrides in the presence of a base. The reaction conditions can be applied to the cross-coupling of tertiary, secondary, and primary Groupa 14 compounds. In most cases, the desired arylated products were obtained in synthetically useful yields. Even in the case of aryl iodides containing OH, NH2, CN, or CO2R groups, the reactions proceeded with good to high yields with tolerance of these reactive functional groups. A possible application of this method is the unique synthesis of a fungicidal diarylmethyl(1H-1,2,4-triazol-1-ylmethyl)silane derivative. A convenient procedure has been developed for the preparation of Groupa 14 compounds by integrated palladium-catalyzed cross-coupling of aromatic iodides with the corresponding Groupa 14 hydrides in the presence of a base (see picture). Application of this method in the synthesis of a fungicidal diarylmethyl(1H-1,2,4-triazol-1-yl-methyl)silane derivative is demonstrated. Copyright