Molecular structure of Bromotriethylsilane, CAS Number: 1112-48-7
Bromotriethylsilane (CAS 1112-48-7)
Alternate Names:
Triethylbromosilane
CAS Number:
1112-48-7
Molecular Weight:
195.17
Molecular Formula:
C6H15BrSi
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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Bromotriethylsilane is primarily used in organic synthesis as a reagent for introducing triethylsilyl groups into molecular structures. This compound is particularly valuable for its role in silylation reactions, where it enhances the stability of sensitive functional groups during synthetic procedures. Research involving Bromotriethylsilane often focuses on its application in protecting groups and its utility in the modification of alcohols, amines, and other reactive moieties. Additionally, Bromotriethylsilane is explored for its effectiveness in promoting cleavage reactions, which are essential for the deprotection and subsequent functionalization of organic molecules.
Bromotriethylsilane (CAS 1112-48-7) References
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- The McKenna reaction - avoiding side reactions in phosphonate deprotection. | Justyna, K., et al. 2020. Beilstein J Org Chem. 16: 1436-1446. PMID: 32647545
- One-Step Synthesis of Triphenylphosphonium Salts from (Het)arylmethyl Alcohols. | Chalikidi, PN., et al. 2021. J Org Chem. 86: 9838-9846. PMID: 34232646
- Iterative addition of carbon nucleophiles to N,N-dialkyl carboxamides for synthesis of α-tertiary amines. | Chen, J., et al. 2021. Chem Sci. 13: 99-104. PMID: 35059156
- Bromotrimethylsilane as a selective reagent for the synthesis of bromohydrins. | Giomi, D., et al. 2021. RSC Adv. 11: 14453-14458. PMID: 35424012
- Copper-Catalyzed Annulation-Trifluoromethyl Functionalization of Enynones. | Wang, JY., et al. 2023. Org Lett. 25: 2509-2514. PMID: 37010156
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| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Bromotriethylsilane, 5 g | sc-227534 | 5 g | $245.00 |