Molecular structure of 4-(Trimethylsilyl)phenylboronic acid, CAS Number: 17865-11-1
4-(Trimethylsilyl)phenylboronic acid (CAS 17865-11-1)
CAS Number:
17865-11-1
Molecular Weight:
194.11
Molecular Formula:
C9H15BO2Si
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
QUICK LINKS
Ordering Information
Description
Technical Information
Safety Information
SDS & Certificate of Analysis
4-(Trimethylsilyl)phenylboronic acid is a white to off-white crystalline substance that readily dissolves in organic solvents like THF, DMSO, and dichloromethane. Thanks to its boronic acid feature, it′s adept at forming temporary covalent connections with biomolecules, including enzymes and receptors, making it invaluable in analyzing biological activities. This compound is frequently used in reactions such as the Suzuki-Miyaura cross-coupling and C-H activation. Apart from its role in synthetic reactions, it acts as an energy acceptor in fluorescence, capable of absorbing and transferring light energy to different molecules. This makes it a pivotal tool for crafting other compounds and delving deeper into biological processes.
4-(Trimethylsilyl)phenylboronic acid (CAS 17865-11-1) References
- Cyclic [2]pseudorotaxane tetramers consisting of two rigid rods threaded through two bis-macrocycles: copper(I)-templated synthesis and X-ray structure studies. | Frey, J., et al. 2008. J Am Chem Soc. 130: 11013-22. PMID: 18652470
- Periodic mesoporous organosilica derivatives bearing a high density of metal complexes on pore surfaces. | Waki, M., et al. 2011. Angew Chem Int Ed Engl. 50: 11667-71. PMID: 22021049
- Photoinduced electron transfer in linear triarylamine-photosensitizer-anthraquinone triads with ruthenium(II), osmium(II), and iridium(III). | Hankache, J., et al. 2012. Inorg Chem. 51: 6333-44. PMID: 22621319
- Twisted polycyclic arenes by intramolecular Scholl reactions of C3-symmetric precursors. | Pradhan, A., et al. 2013. J Org Chem. 78: 2266-74. PMID: 23374076
- Extending the limits of precision polymer synthesis: giant polyphenylene dendrimers in the megadalton mass range approaching structural perfection. | Nguyen, TT., et al. 2013. J Am Chem Soc. 135: 4183-6. PMID: 23451994
- Scope and Limitations of the Liebeskind-Srogl Cross-Coupling Reactions Involving the Biellmann BODIPY. | Betancourt-Mendiola, L., et al. 2015. J Org Chem. 80: 5771-82. PMID: 25965325
- Self-Assembly of a Tripod Aromatic Rod into Stacked Planar Networks. | Kim, HJ., et al. 2015. Chemistry. 21: 11836-42. PMID: 26147242
- From Blue to Green: Fine-Tuning of Photoluminescence and Electrochemiluminescence in Bifunctional Organic Dyes. | Rizzo, F., et al. 2017. J Am Chem Soc. 139: 2060-2069. PMID: 28088858
- Morphological Control of Coil-Rod-Coil Molecules Containing m-Terphenyl Group: Construction of Helical Fibers and Helical Nanorings in Aqueous Solution. | Yang, Y., et al. 2018. Langmuir. 34: 10613-10621. PMID: 30107734
- Selective Synthesis of ortho-Substituted Diarylsulfones by Using NHC-Au Catalysts under Mild Conditions. | Zhu, H., et al. 2019. Org Lett. 21: 974-979. PMID: 30702302
- Supramolecular Nanopumps with Chiral Recognition for Moving Organic Pollutants from Water. | Bao, S., et al. 2019. ACS Appl Mater Interfaces. 11: 31220-31226. PMID: 31380620
- Nickel-Catalyzed Arylative Cyclizations of Alkyne- and Allene-Tethered Electrophiles using Arylboron Reagents. | Gillbard, SM. and Lam, HW. 2022. Chemistry. 28: e202104230. PMID: 34986277
- Improvement of the fluorescence quantum yield of triphenylene by the rotational effect of 4-(trimethylsilyl) phenyl groups. | Kyushin, S., Fujii, H., Negishi, K., & Matsumoto, H. 2022. Mendeleev Communications. 32(1): 87-90.
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
4-(Trimethylsilyl)phenylboronic acid, 1 g | sc-226454 | 1 g | $74.00 |