Triethoxy-p-tolylsilane (CAS 18412-57-2)
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Triethoxy-p-tolylsilane is an organosilicon compound with diverse applications in the chemical industry. It consists of a p-tolyl group, an oxygen atom, and three ethoxy groups. Triethoxy-p-tolylsilane presents itself as a colorless and odorless liquid. This compound exhibits solubility in both water and organic solvents. Triethoxy-p-tolylsilane finds extensive use in scientific research endeavors. It plays a role in the synthesis of polysiloxanes, which serve as the building blocks for various silicone-based materials. Moreover, it contributes to the production of silane-based polymers and monomers, which find applications in coatings, adhesives, and other materials. Additionally, Triethoxy-p-tolylsilane is instrumental in the synthesis of organosilicon compounds. As an organosilicon compound, Triethoxy-p-tolylsilane encompasses both carbon and silicon atoms. The carbon atoms form a chain structure, while the silicon atoms create a network of interconnected bonds.
Triethoxy-p-tolylsilane (CAS 18412-57-2) References
- Precise Stepwise Synthesis of Donor-Acceptor Conjugated Polymer Brushes Grafted from Surfaces. | Grobelny, A., et al. 2022. Int J Mol Sci. 23: PMID: 35682845
- Tunability of Hybrid Silica Xerogels: Surface Chemistry and Porous Texture Based on the Aromatic Precursor. | Rosales-Reina, B., et al. 2023. Gels. 9: PMID: 37232974
- Solvent-free copper/iron co-catalyzed N-arylation reactions of nitrogen-containing heterocycles with trimethoxysilanes in air | Ren-Jie Song, Chen-Liang Deng, Ye-Xiang Xie, Jin-Heng Li. 2007. Tetrahedron Letters. 48: 7845-7848.
- Palladium-catalyzed decarboxylative coupling of benzoic acid derivatives using hydrazone ligands | Takashi Mino, Eri Yoshizawa, Kohei Watanabe, Taichi Abe, Kiminori Hirai, Masami Sakamoto. 2014. Tetrahedron Letters. 55: 3184-3188.
- Competition between the Hiyama and Suzuki–Miyaura Pd-catalyzed cross-coupling reaction mechanisms for the formation of some regioselective derivatives of quinoxaline and benzofuran; Which reaction mechanism is more favorable? | Zeinab Ahmadvand, Mehdi Bayat. 2021. Journal of Molecular Liquids. 325.
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Triethoxy-p-tolylsilane, 1 g | sc-251315 | 1 g | $60.00 |