18415-18-4

Basic information

• Product Name: (1-octyl)(phenyl)silane
• Synonyms: (1-octyl)(phenyl)silane
• CAS NO: 18415-18-4
• Molecular Weight: 220.43
• Mol File: 18415-18-4.mol
• Article Data: 44

Chemical Properties

• CAS DataBase Reference: (1-octyl)(phenyl)silane(CAS DataBase Reference)
• NIST Chemistry Reference: (1-octyl)(phenyl)silane(18415-18-4)
• EPA Substance Registry System: (1-octyl)(phenyl)silane(18415-18-4)

Safety Data

• Hazardous Substances Data: 18415-18-4(Hazardous Substances Data)

Upstream product

• 111-66-0 oct-1-ene 
• 694-53-1 phenylsilane 
• 614-45-9 tert-Butyl peroxybenzoate 
• 110-05-4 di-tert-butyl peroxide 
• 872-05-9 1-Decene 
• 775-12-2 diphenylsilane 

Relevant articles and documents

Thermally Stable Rare-Earth Metal Complexes Supported by Chelating Silylene Ligands

The use of N-heterocyclic silylenes (NHSi) as ligands is a rapidly developing field. However, only a handful of f-element silylene complexes have been disclosed so far. Herein, we report the synthesis and characterization of a series of thermally stable d

Metal-free photocatalytic hydrosilylation of olefins in the presence of photoinitiators

A convenient metal-free photocatalytic hydrosilylation of a variety of linear and cyclic alkenes has been investigated. It was found that the free radical type photoinitiator Irgacure 2959 had a better effect on the hydrosilylation reaction; using 3 mol%

Highly active cobalt complex catalysts used for alkene hydrosilylation

A series of nitrogen phosphine ligands were synthesized, and the hydrosilylation reaction of alkenes catalyzed using MCl2 in the presence of these ligands was investigated. FeCl2/1(N1, N1, N2, N2-Tetrakis[(diphenylphosphino)methyl]ethane-1,2-diamine) showed low catalytic activity. MnCl2/1, CrCl3/1 and NiCl2/1 showed some catalytic activity. The CoCl2/N,P-ligand catalyst system showed high activity as well as excellent selectivity (The selectivity of the β-adduct was ~100%.) in the hydrosilylation reaction. CoCl2/1 showed the highest catalytic activity (~ >99.9% conversion of 1-octene). Additionally, no α-adduct, dehydrogenative silylation product and octane were detected.