4556-72-3

Basic information

• Product Name: (4 - vinyl phenyl) dimethyl silane
• Synonyms: (4 - vinyl phenyl) dimethyl silane;Dimethyl(4-vinylphenyl)silane;(p-Vinylphenyl) Dimethylsilane;(4-ethenylphenyl)-dimethylsilane
• CAS NO: 4556-72-3
• Molecular Formula: C₁₀H₁₄Si
• Molecular Weight: 162.30366
• EINECS: -0
• Mol File: 4556-72-3.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• CAS DataBase Reference: (4 - vinyl phenyl) dimethyl silane(CAS DataBase Reference)
• NIST Chemistry Reference: (4 - vinyl phenyl) dimethyl silane(4556-72-3)
• EPA Substance Registry System: (4 - vinyl phenyl) dimethyl silane(4556-72-3)

Safety Data

• Hazardous Substances Data: 4556-72-3(Hazardous Substances Data)

Usage

General Description

(4-vinyl phenyl) dimethyl silane is an organosilicon compound with the chemical formula C10H14Si. It is a colorless liquid with a slightly sweet odor and is used in the production of silicones and as a crosslinking agent in the synthesis of polymers. It is also used as a reagent in organic synthesis, particularly in the formation of carbon-silicon bonds. (4-vinyl phenyl) dimethyl silane is flammable and should be handled with care due to its potential health hazards. It is important to use proper safety precautions when working with this chemical to minimize potential risks.

Upstream product

• 1066-35-9 dimethylmonochlorosilane 
• 2039-82-9 1-bromo-4-ethenyl-benzene 
• 1073-67-2 4-vinylbenzyl chloride 

Downstream Products

• 57295-14-4 tert-butyl 4-vinylphenylcarbamate 

Relevant articles and documents

Synthesis and characterization of in-chain silyl-hydride functional SBR and self-crosslinking elastomer

Functional in-chain silyl-hydride (Si-H) SBR copolymers of 4-vinyiphenyldimethylsilanol (VPDMS) and butadiene were synthesized by living anionic polymerization, in which active group Si-H was not lost and its content was controllable. Corresponding self-c

Selective Manganese-Catalyzed Oxidation of Hydrosilanes to Silanols under Neutral Reaction Conditions

The first manganese-catalyzed oxidation of organosilanes to silanols with H2O2 under neutral reaction conditions has been accomplished. A variety of organosilanes with alkyl, aryl, alknyl, and heterocyclic substituents were tolerated, as well as sterically hindered organosilanes. The oxidation appears to proceed by a concerted process involving a manganese hydroperoxide species. Featuring mild reaction conditions, fast oxidation, and no waste byproducts, the protocol allows a low-cost, eco-benign synthesis of both silanols and silanediols.