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Atomfair 4,4,5,5-Tetramethyl-2-(prop-1-en-2-yl)-1,3,2-dioxaborolane C9H17BO2

Description 4,4,5,5-Tetramethyl-2-(prop-1-en-2-yl)-1,3,2-dioxaborolane (CAS No. 126726-62-3) is a highly versatile boronic ester compound with the molecular formula C9H17BO2. This organoboron reagent features a stable dioxaborolane ring system with tetramethyl substitution, enhancing its reactivity and stability for cross-coupling reactions. It is widely used in Suzuki-Miyaura coupling, a pivotal reaction in pharmaceutical and materials science research. The compound is supplied as a clear to pale yellow liquid, stored under inert conditions to ensure purity and longevity. Ideal for advanced synthetic applications, it is a critical building block for constructing complex organic molecules.

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Description

Description

4,4,5,5-Tetramethyl-2-(prop-1-en-2-yl)-1,3,2-dioxaborolane (CAS No. 126726-62-3) is a highly versatile boronic ester compound with the molecular formula C9H17BO2. This organoboron reagent features a stable dioxaborolane ring system with tetramethyl substitution, enhancing its reactivity and stability for cross-coupling reactions. It is widely used in Suzuki-Miyaura coupling, a pivotal reaction in pharmaceutical and materials science research. The compound is supplied as a clear to pale yellow liquid, stored under inert conditions to ensure purity and longevity. Ideal for advanced synthetic applications, it is a critical building block for constructing complex organic molecules.

  • CAS No: 126726-62-3
  • Molecular Formula: C9H17BO2
  • Molecular Weight: 168.04
  • Exact Mass: 168.1321599
  • Monoisotopic Mass: 168.1321599
  • IUPAC Name: 4,4,5,5-tetramethyl-2-prop-1-en-2-yl-1,3,2-dioxaborolane
  • SMILES: B1(OC(C(O1)(C)C)(C)C)C(=C)C
  • Synonyms: 126726-62-3, 4,4,5,5-tetramethyl-2-(prop-1-en-2-yl)-1,3,2-dioxaborolane, DTXSID70451202, DTXCID20402022, 627-007-7

Application

This compound is extensively utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to form carbon-carbon bonds. It serves as a key intermediate in the preparation of pharmaceuticals, agrochemicals, and advanced materials. Researchers value its stability and reactivity in palladium-catalyzed transformations. It is also employed in the synthesis of boron-containing polymers and ligands for catalysis.

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