120578-34-9

Basic information

• Product Name: Silane, (2,4,6-trimethylphenyl)-
• CAS NO: 120578-34-9
• Molecular Formula: C9H14Si
• Molecular Weight: 150.296
• Mol File: 120578-34-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Silane, (2,4,6-trimethylphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Silane, (2,4,6-trimethylphenyl)-(120578-34-9)
• EPA Substance Registry System: Silane, (2,4,6-trimethylphenyl)-(120578-34-9)

Safety Data

• Hazardous Substances Data: 120578-34-9(Hazardous Substances Data)

Upstream product

• 17902-75-9 2,4,6-trimethyl-phenyl-trichlorosilane 
• 198883-34-0 chloro(mesityl)silane 

Downstream Products

• 1072936-12-9 [(C₅H₅)(1,2-bis(dimethylphosphino)ethane)VSiH₂(2,4,6-Me₃C₆H₃)] 
• 1179317-11-3 H₂SiMes(CH₂CH₂PhCl) 
• 1042011-30-2 H₂SiMes(Hex) 
• 1179317-12-4 H₂SiMes(CH₂CH₂SiMe₃) 
• 139039-99-9 1,2-dimesityldisilane 
• 99798-82-0 bis(2,4,6-trimethyphenyl)silane 
• 1450594-40-7 C₁₄H₂₂Si 
• 13966-57-9 chlorosilane 
• 4109-96-0 Dichlorosilane 
• 1414859-90-7 C₁₃H₂₃NSi 
• 95599-69-2 bis(mesityl)silanediol 
• 1320352-60-0 (2,6-bis(trifluoromethyl)phenyl)(mesityl)silanediol 

Relevant articles and documents

Carbon-Silicon Bond Formation in the Synthesis of Benzylic Silanes

Sterically encumbered organosilanes can be difficult to synthesize with conventional, strongly basic reagents; the harsh reaction conditions are often low yielding and not suitable for many functional groups. As an alternative to the typical anionic strat

Synthesis, structure and photoluminescence of 1,2-disila-acenaphthene Si2C10H10 and 1,2-diaryldisilane reference compounds

For the synthesis of the diaryldisilanes Ar-SiH2SiH2-Ar (la, Ar = phenyl; Ib, Ar = p-tolyl; le, Ar = mesityl; Id, Ar = p-anisyl) two convenient preparative routes are reported. The crystal structures of le and Id have been determined in Xray diffraction studies; the disilanes have a staggered transconformation with a crystallographically imposed center of inversion. For la-d no photoluminescence phenomena can be observed. 1,2-Disila-acenaphthene (2) is synthesized in acceptable yield by treatment of 1,8-dilithionaphthalene with 1 equivalent of l,2-bis[((trifluoromethyl)sulfonyl)oxy]disilane Tf-SiH2SiH2-Tf. The crystal structure of 2 has also been determined by X-ray diffraction. The molecule has no crystallographically imposed symmetry but closely follows the symmetry elements of point group C2v. Solutions of 2 exhibit intense fluorescence in the near UV region at room temperature. The fluorescence spectra are discussed in comparison with data on acenaphthene and naphthalene. WILEY-VCH Verlag GmbH 1997.