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Atomfair 2-Isopropoxy-4,4,6-trimethyl-1,3,2-dioxaborinane C9H19BO3

Description 2-Isopropoxy-4,4,6-trimethyl-1,3,2-dioxaborinane (CAS: 61676-61-7) is a highly specialized organoboron compound with the molecular formula C9H19BO3. This cyclic boronic ester features a dioxaborinane core substituted with isopropoxy and three methyl groups, offering unique reactivity and stability for advanced synthetic applications. The compound is supplied as a high-purity liquid (typically >95% by GC) with careful handling recommended due to its moisture sensitivity. Researchers value this chemical for its role as a versatile intermediate in cross-coupling reactions, particularly in Suzuki-Miyaura couplings where its sterically hindered structure can influence selectivity. The product is packaged under inert gas in amber glass bottles with secure closures…

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Description

Description

2-Isopropoxy-4,4,6-trimethyl-1,3,2-dioxaborinane (CAS: 61676-61-7) is a highly specialized organoboron compound with the molecular formula C9H19BO3. This cyclic boronic ester features a dioxaborinane core substituted with isopropoxy and three methyl groups, offering unique reactivity and stability for advanced synthetic applications. The compound is supplied as a high-purity liquid (typically >95% by GC) with careful handling recommended due to its moisture sensitivity. Researchers value this chemical for its role as a versatile intermediate in cross-coupling reactions, particularly in Suzuki-Miyaura couplings where its sterically hindered structure can influence selectivity. The product is packaged under inert gas in amber glass bottles with secure closures to ensure maximum shelf life and is ideal for pharmaceutical research, materials science, and catalytic system development.

  • CAS No: 61676-61-7
  • Molecular Formula: C9H19BO3
  • Molecular Weight: 186.06
  • Exact Mass: 186.1427246
  • Monoisotopic Mass: 186.1427246
  • IUPAC Name: 4,4,6-trimethyl-2-propan-2-yloxy-1,3,2-dioxaborinane
  • SMILES: B1(OC(CC(O1)(C)C)C)OC(C)C
  • Synonyms: 2-ISOPROPOXY-4,4,6-TRIMETHYL-1,3,2-DIOXABORINANE, 636-406-5, 61676-61-7, 1,3,2-Dioxaborinane, 4,4,6-trimethyl-2-(1-methylethoxy)-, 2-isopropoxy-4,4,6-trimethyl-[1,3,2]dioxaborinane

Application

This boronic ester serves as a key intermediate in palladium-catalyzed cross-coupling reactions for constructing complex organic molecules. Its sterically demanding structure makes it particularly useful for synthesizing hindered biaryl compounds in medicinal chemistry applications. The compound has shown utility in polymer chemistry as a modifying agent for resins and as a precursor for boron-containing materials. Researchers also employ it in the development of new catalytic systems for asymmetric synthesis.

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