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Atomfair 4,4,5,5-Tetramethyl-2-(thiophen-3-yl)-1,3,2-dioxaborolane C10H15BO2S
Description 4,4,5,5-Tetramethyl-2-(thiophen-3-yl)-1,3,2-dioxaborolane (CAS No. 214360-70-0) is a high-purity boronic ester derivative with the molecular formula C10H15BO2S . This compound features a thiophene moiety coupled to a dioxaborolane ring, making it a valuable intermediate in organic synthesis and cross-coupling reactions. Its rigid, sterically hindered structure enhances stability, ensuring reliable performance in Suzuki-Miyaura and other palladium-catalyzed transformations. Ideal for researchers in pharmaceuticals, agrochemicals, and materials science, this reagent is supplied as a crystalline solid with ??95% purity (GC). Store under inert conditions to maintain reactivity and shelf life. Available in scalable quantities with comprehensive analytical data (NMR, HPLC, MS) for quality assurance.
Description
Description
4,4,5,5-Tetramethyl-2-(thiophen-3-yl)-1,3,2-dioxaborolane (CAS No. 214360-70-0) is a high-purity boronic ester derivative with the molecular formula C10H15BO2S. This compound features a thiophene moiety coupled to a dioxaborolane ring, making it a valuable intermediate in organic synthesis and cross-coupling reactions. Its rigid, sterically hindered structure enhances stability, ensuring reliable performance in Suzuki-Miyaura and other palladium-catalyzed transformations. Ideal for researchers in pharmaceuticals, agrochemicals, and materials science, this reagent is supplied as a crystalline solid with ??95% purity (GC). Store under inert conditions to maintain reactivity and shelf life. Available in scalable quantities with comprehensive analytical data (NMR, HPLC, MS) for quality assurance.
- CAS No: 214360-70-0
- Molecular Formula: C10H15BO2S
- Molecular Weight: 210.11
- Exact Mass: 210.0885811
- Monoisotopic Mass: 210.0885811
- IUPAC Name: 4,4,5,5-tetramethyl-2-thiophen-3-yl-1,3,2-dioxaborolane
- SMILES: B1(OC(C(O1)(C)C)(C)C)C2=CSC=C2
- Synonyms: 214360-70-0, 4,4,5,5-tetramethyl-2-(thiophen-3-yl)-1,3,2-dioxaborolane, DTXSID10375251, DTXCID30326280, 674-923-8
Application
4,4,5,5-Tetramethyl-2-(thiophen-3-yl)-1,3,2-dioxaborolane is widely used as a key building block in Suzuki-Miyaura cross-coupling reactions to synthesize biaryl compounds for drug discovery. Its thiophene-boronate structure facilitates the introduction of sulfur-containing heterocycles into complex molecules, enhancing electronic properties in organic semiconductors. This reagent is also employed in the development of conjugated polymers and advanced materials for optoelectronic applications.
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