Molecular structure of Trimethyl(phenyl)silane, CAS Number: 768-32-1
Trimethyl(phenyl)silane (CAS 768-32-1)
Alternate Names:
(Trimethylsilyl)benzene; Phenyltrimethylsilane
CAS Number:
768-32-1
Molecular Weight:
150.29
Molecular Formula:
C9H14Si
Supplemental Information:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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Trimethyl(phenyl)silane, also known as PhenyltriMethylsilane is a reagent used in the creation of organic compounds. It′s a tri-methylsilane that possesses a phenyl group linked to one of its methyl segments. With an intrinsic hydroxyl group and UV absorption bands at both 330 nm and 240 nm, it serves as a probe for magnetic resonance spectroscopy. This compound also acts as an intermediate in organic synthesis.
Trimethyl(phenyl)silane (CAS 768-32-1) References
- Plasmon waveguide resonance Raman spectroscopy. | McKee, KJ., et al. 2012. Anal Chem. 84: 9049-55. PMID: 23046486
- Asymmetric δ-Lactam Synthesis with a Monomeric Streptavidin Artificial Metalloenzyme. | Hassan, IS., et al. 2019. J Am Chem Soc. 141: 4815-4819. PMID: 30865436
- Catalytically Generated Meerwein's Salt-Type Oxonium Ions for Friedel-Crafts C(sp2)-H Methylation with Methanol. | He, T., et al. 2023. J Am Chem Soc. 145: 3795-3801. PMID: 36724501
- Co-Condensation Reactions of Substituted Aromatic Compounds with Lithium Atoms at 77 K | John P. Dunne, Matthias Bockmeyer, Matthias Tacke. 2003. European Journal of Inorganic Chemistry. 2003: 458-466.
- Phenylsilane; unreactive group in the metallocene/MAO catalyzed copolymerization of propylene and 7-octenyldimethylphenylsilane, reactive group in melt blending with microsilica filler | Sami Lipponen, Mika Lahelin, Jukka Seppälä. 2009. European Polymer Journal. 45: 1179-1189.
- Trimethyl(phenyl)silane - a precursor for gas phase processes of SiCx:H film deposition: Synthesis and characterization | Evgeniya N. Ermakova a, Sergey V. Sysoev a, Lyubov' D. Nikulina a, Irina P. Tsyrendorzhieva b, Vladimir I. Rakhlin b, Marina L. Kosinova a. 2015. Modern Electronic Materials. 1: 114-119.
- Flexible Reaction Pocket on Bulky Diphosphine–Ir Complex Controls Regioselectivity in para-Selective C–H Borylation of Arenes | Brandon E. Haines†, Yutaro Saito‡, Yasutomo Segawa‡∥, Kenichiro Itami*‡∥§, and Djamaladdin G. Musaev*†. 2016. ACS Catal. 6: 7536–7546.
- Thermal properties of some organosilicon precursors for chemical vapor deposition | E. N. Ermakova, S. V. Sysoev, R. E. Nikolaev, L. D. Nikulina, A. V. Lis, I. P. Tsyrendorzhieva, V. I. Rakhlin, P. E. Plyusnin & M. L. Kosinova. 2016. Journal of Thermal Analysis and Calorimetry. 126: 609–616.
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Trimethyl(phenyl)silane, 25 g | sc-251355 | 25 g | $112.00 |