17908-86-0

Basic information

• Product Name: benzyloxydimethylphenylsilane
• Synonyms: benzyloxydimethylphenylsilane
• CAS NO: 17908-86-0
• Molecular Weight: 242.393
• Mol File: 17908-86-0.mol
• Article Data: 51

Chemical Properties

• CAS DataBase Reference: benzyloxydimethylphenylsilane(CAS DataBase Reference)
• NIST Chemistry Reference: benzyloxydimethylphenylsilane(17908-86-0)
• EPA Substance Registry System: benzyloxydimethylphenylsilane(17908-86-0)

Safety Data

• Hazardous Substances Data: 17908-86-0(Hazardous Substances Data)

Upstream product

• 201230-82-2 carbon monoxide 
• 766-77-8 Dimethylphenylsilane 
• 100-52-7 benzaldehyde 
• 100-51-6 benzyl alcohol 
• 1927-62-4 tetrahydro-2-(benzyloxy)-2H-pyran 
• 185990-03-8 dimethylphenyl(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)silane 
• 98-88-4 benzoyl chloride 
• 768-33-2 phenyldimethylsilyl chloride 
• 13959-92-7 benzyl triethylsilyl ether 
• 14642-79-6 benzyloxy-trimethylsilane 
• 1125-26-4 dimethylphenylvinylsilane 
• 2923-28-6 silver trifluoromethanesulfonate 

Downstream Products

• 135987-50-7 (+/-)-1-phenyl-1-(dimethylphenylsilyl)methanol 
• 5272-18-4 dimethylphenylsilanol 
• 56-33-7 1,1,3,3-tetramethyl-1,3-diphenyldisiloxane 
• 14920-92-4 pentamethyl(phenyl)disiloxane 
• 108-88-3 toluene 
• 100-51-6 benzyl alcohol 

Relevant articles and documents

Enhanced catalytic activity of self-assembled-monolayer-capped gold nanoparticles

An unprecedented substrate-selective catalytic enhancement effect of an alkanethiol-self-assembled monolayer (SAM) on Au nanoparticles (AuNPs) is reported. In the supported 2D-array of AuNPs, the alkanethiol-SAM acts as a protein-like soft reaction space

Use of Silylated Formiates as Hydrosilane Equivalents

The present invention relates to a method for preparing organic compounds of formula (I) by reaction between a silylated formiate of formula (II) and an organic compound in the presence of a catalyst and optionally of an additive. The invention also relates to use of the method for preparing organic compounds of formula (I) for the preparation of reagents for fine chemistry and for heavy chemistry, as well as in the production of vitamins, pharmaceutical products, adhesives, acrylic fibres, synthetic leathers, and pesticides.

Photoactivated silicon-oxygen and silicon-nitrogen heterodehydrocoupling with a commercially available iron compound

Silicon-oxygen and silicon-nitrogen heterodehydrocoupling catalyzed by the commercially available cyclopentadienyl dicarbonyl iron dimer [CpFe(CO)2]2 (1) under photochemical conditions is reported. Reactions between alcohols and PhSi