56318-71-9

Basic information

• Product Name: N-DECYLDIMETHYLSILANE
• Synonyms: decyldimethyl-silan;N-DECYLDIMETHYLSILANE;decyldimethylsilane
• CAS NO: 56318-71-9
• Molecular Formula: C₁₂H₂₈Si
• Molecular Weight: 200.44
• EINECS: 260-109-6
• Mol File: 56318-71-9.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 229.1 °C at 760 mmHg
• Flash Point: 82.8 °C
• Appearance: /
• CAS DataBase Reference: N-DECYLDIMETHYLSILANE(CAS DataBase Reference)
• NIST Chemistry Reference: N-DECYLDIMETHYLSILANE(56318-71-9)
• EPA Substance Registry System: N-DECYLDIMETHYLSILANE(56318-71-9)

Safety Data

• Hazardous Substances Data: 56318-71-9(Hazardous Substances Data)

Usage

General Description

N-Decyldimethylsilane is a chemical compound with the formula C12H28Si. It is classified as a silane, which is a type of organosilicon compound that contains silicon and carbon atoms bonded together. N-Decyldimethylsilane is commonly used as a surface modification agent, as it can be applied to various substrates to provide water repellency and enhance adhesion properties. It is also utilized as a building block in the synthesis of other organosilicon compounds and in the production of silicone-based materials. Additionally, N-Decyldimethylsilane has potential applications in the field of drug delivery systems and as a reactive intermediate in organic synthesis. Due to its chemical properties and versatility, it is a valuable component in various industrial and research processes.

InChI:InChI=1/C12H27Si/c1-4-5-6-7-8-9-10-11-12-13(2)3/h4-12H2,1-3H3

Upstream product

• 1066-35-9 dimethylmonochlorosilane 
• 17049-50-2 n-decyl magnesium bromide 
• 872-05-9 1-Decene 
• 18033-75-5 dimethylmethoxysilane 
• 112-29-8 1-bromo dodecane 
• 38051-57-9 N-decyldimethylchlorosilane 

Downstream Products

• 56318-63-9 Decyl-dimethyl-pentafluorophenyloxy-silane 
• 112-30-1 1-Decanol 
• 38051-57-9 N-decyldimethylchlorosilane 

Relevant articles and documents

Alkoxy Hydrosilanes As Surrogates of Gaseous Silanes for Hydrosilylation of Alkenes

Me2SiH2, MeSiH3, and SiH4 are gaseous and flammable silanes that are inconvenient to use in chemical reactions. Catalytic amounts of a nickel pincer complex and NaOtBu are reported to allow the synthesis of alkyl hydrosilanes from alkenes and alkoxy hydrosilanes, leading to the replacement of Me2SiH2, MeSiH3, and SiH4 by Me2(MeO)SiH, Me(EtO)2SiH, and (MeO)3SiH in hydrosilylation reactions of alkenes. The scope and mechanism of the reactions are also described.

Predictability of thermal and electrical properties of end-capped oligothiophenes by a simple bulkiness parameter

The branching topology of end groups attached to several series of oligothiophenes has a systematic effect on thermal and electrical properties of the oligomers. The series were synthesized in a modular approach and show a distinct drop of the melting point Tm on increasing bulkiness of the substituents. The same trend can be found for the dissociation temperatures Tdis of aggregates in solution. Similarly, monolayer OFET mobilities μFET are significantly decreasing with increasing bulkiness of the substituents. A simple geometric model is presented quantitatively correlating the transition temperatures and mobilities with the substituents' structure based on a bulkiness parameter P, which allows predicting Tm, T dis, and μFET of corresponding not yet synthesized oligomers with branched substituents. This model might be generally applicable for end-capped rod-like conjugated oligomers.