130255-43-5

Basic information

• Product Name: bis(dimethyl(phenyl)silyl)methanone
• Synonyms: bis(dimethyl(phenyl)silyl)methanone
• CAS NO: 130255-43-5
• Molecular Weight: 298.532
• Mol File: 130255-43-5.mol

Chemical Properties

• CAS DataBase Reference: bis(dimethyl(phenyl)silyl)methanone(CAS DataBase Reference)
• NIST Chemistry Reference: bis(dimethyl(phenyl)silyl)methanone(130255-43-5)
• EPA Substance Registry System: bis(dimethyl(phenyl)silyl)methanone(130255-43-5)

Safety Data

• Hazardous Substances Data: 130255-43-5(Hazardous Substances Data)

Upstream product

• 183372-74-9 2,2-bis(dimethylphenylsilyl)-1,3-dioxolane 
• 768-33-2 phenyldimethylsilyl chloride 

Downstream Products

• 130255-48-0 (Z)-1,2-Bis-(dimethyl-phenyl-silanyl)-hept-2-en-1-one 
• 130255-47-9 3,3-Bis-(dimethyl-phenyl-silanyl)-3-hydroxy-propionic acid ethyl ester 
• 1152097-25-0 C₁₉H₂₈OSSi₂ 
• 1152097-24-9 C₂₆H₃₂OSSi₂ 
• 1152097-23-8 C₂₃H₂₈OSSi₂ 
• 1152097-21-6 C₂₄H₃₀OSi₂ 
• 1152097-22-7 C₂₃H₂₈OSi₂ 
• 503607-18-9 3-[dimethyl(phenyl)silyl]-3-[dimethyl(phenyl)silyloxy]-4-phenylbut-1-ene 
• 1152097-27-2 C₉H₁₃NOSi 
• 474662-63-0 C₂₃H₂₈OSi₂ 
• 1152097-20-5 C₁₈H₂₆OSi₂ 
• 130255-51-5 1,1-bisethanol 
• 1152097-26-1 C₁₈H₂₃NOSi₂ 
• 130255-49-1 ethene-1,1-diylbis(dimethyl(phenyl)silane) 

Relevant articles and documents

DENTAL COMPOSITION

Photocurable dental composition comprising (a) one or more radical-polymerizable monomers, and (b) 0.1 to 7.0 percent by weight based on the total weight of radical polymerizable monomers in the composition of a compound of the following formula (I): Rsu

Studies on the 1,2-brook rearrangement of bissilyl ketones

The first 1,2-Brook rearrangements with bis(dimethylphenylsilyl) ketone, initiated after addition of different C- and S-nucleophiles, are described. The resulting, newly formed carbanion can be trapped with electrophiles thus paving the way for utilizing bissilyl ketones as formyl dianion equivalents in the future. Georg Thieme Verlag Stuttgart.

Bissilyl ketone; A convenient method for the synthesis and its Pd(0) catalyzed reaction with alkenes and alkynes

A convenient method for the preparation of a bissilyl ketone is developed via a bissilyl ketone acetal as its precursor. The bissilyl ketone reacts with electron deficient alkynes and alkenes in the presence of Pd(0) catalyst to give bis-silylated products.

Synthesis, Molecular Structure, and Some Reactions of Bis(dimethylphenylsilyl)Ketone

The title compound was prepared from bis(methylthio)methane as a crystalline compound.The molecular structure was determined by X-ray crystallographic analysis, and reactions with alkyl metals and a Wittig reagent were examined.