13617-28-2

Basic information

• Product Name: (3-PHENYLPROPYL)METHYLDICHLOROSILANE
• Synonyms: (2-Phenyl-2-methylethyl)methyldichlorosilane;dichloromethyl(2-phenylpropyl)-silan;Silane, dichloromethyl(2-phenylpropyl)-;(3-PHENYLPROPYL)METHYLDICHLOROSILANE;(2-METHYL-2-PHENYLETHYL)METHYLDICHLOROSILANE;METHYL(2-PHENYLPROPYL)DICHLOROSILANE;METHYL (3-PHENYLPROPYL ) DICHLOROSILANE;dichloromethyl(2-phenylpropyl)silane
• CAS NO: 13617-28-2
• Molecular Formula: C₁₀H₁₄Cl₂Si
• Molecular Weight: 233.21
• EINECS: 237-102-1
• Mol File: 13617-28-2.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 94-96°C 3,8mm
• Flash Point: 98 °C
• Appearance: /
• Density: 1,116 g/cm3
• Vapor Pressure: 0.0432mmHg at 25°C
• Refractive Index: 1.5152
• CAS DataBase Reference: (3-PHENYLPROPYL)METHYLDICHLOROSILANE(CAS DataBase Reference)
• NIST Chemistry Reference: (3-PHENYLPROPYL)METHYLDICHLOROSILANE(13617-28-2)
• EPA Substance Registry System: (3-PHENYLPROPYL)METHYLDICHLOROSILANE(13617-28-2)

Safety Data

• Statements: 34
• Safety Statements: 26-36/37/39
• RIDADR: 2987
• TSCA: Yes
• Hazardous Substances Data: 13617-28-2(Hazardous Substances Data)

Usage

General Description

"(3-Phenylpropyl)Methyldichlorosilane" is a specific type of organosilicon compound that is composed of carbon, hydrogen, chlorine, and silicon atoms. This chemical has various commercial and industrial applications, primarily in the field of material sciences and chemical synthesis. It is generally utilized as an intermediate reagent for the development of more complex organic molecules. The presence of both silane and phenyl groups in "(3-Phenylpropyl)Methyldichlorosilane" allows it to participate in multiple types of chemical reactions, thereby increasing its versatility as a reagent. Although hazardous if improperly handled, under controlled conditions, it is considered a valuable resource in synthetic chemistry.

InChI:InChI=1/C10H14Cl2Si/c1-9(8-13(2,11)12)10-6-4-3-5-7-10/h3-7,9H,8H2,1-2H3

Upstream product

• 7787-92-0 dichloro-(2-chloro-propyl)-methyl-silane 
• 71-43-2 benzene 
• 75-54-7 Dichloromethylsilane 
• 98-83-9 isopropenylbenzene 
• 7787-93-1 dichloro(3-chloropropyl)methylsilane 

Downstream Products

• 18027-28-6 trimethyl(2-phenylpropyl)silane 
• 28455-47-2 2,4,6-Trimethyl-2,4,6-tris-(2-phenyl-propyl)-[1,3,5,2,4,6]triazatrisilinane 
• 27329-85-7 2,4,6-Trimethyl-2,4,6-tris-(2-phenyl-propyl)-[1,3,5,2,4,6]trithiatrisilinane 
• 347194-22-3 dimethoxymethyl(2-phenylpropyl)silane 
• 34074-21-0 methoxydimethyl(2-phenylpropyl)silane 
• 347194-23-4 fluorodimethyl(2-phenylpropyl)silane 
• 18758-65-1 2,4,6-trimethyl-2,4,6-tris-(2-phenyl-propyl)-cyclotrisiloxane 

Relevant articles and documents

Hydrosilylation of 2-Phenylpropene with dichloromethylsilane and transformations of the resulting adduct

2-Phenylpropene was hydrosilylated with dichloromethylsilane in the presence of H2PtCl6 to synthesize dichloromethyl(2-phenylpropyl)silane. The latter was reacted with methanol in the presence of carbamide to obtain dimethoxymethyl(2-phenylpropyl)silane, whose reaction with methylmagnesium iodide gave methoxydimethyl(2-phenylpropyl)silane. Treatment of the latter with 40% HF gave fluorodimethyl(2-phenylpropyl)silane which was reacted with BrMgC≡CH to obtain dimethylethynyl(2-phenylpropyl)silane.

Process for the preparation of organosilicon compounds

This invention relates to the preparation of organosilicon compounds by the addition of a silicon compound containing Si-bonded hydrogen to a compound having an aliphatic multiple bond in the presence of a catalyst which promotes the addition of Si-bonded hydrogen to compounds containing an aliphatic multiple bond. In this process the reactants and the catalyst are continuously introduced into a pipe-shaped reactor while the contents of the reactor, which are maintained in a liquid phase by the application of pressure are circulated in the reactor at a rate of at least 1,000 cm per minute and while the reaction mixture is continuously being removed from the reactor.