Description

4,4,6-Trimethyl-1,3,2-dioxaborinane (CAS No. 23894-82-8) is a specialized cyclic boronic ester with the molecular formula C₆H₁₂BO₂. This high-purity compound is widely utilized in organic synthesis, pharmaceutical research, and materials science due to its unique reactivity as a boron-containing intermediate. The dioxaborinane structure, featuring three methyl groups at the 4,4,6-positions, offers enhanced stability and controlled reactivity for cross-coupling reactions, Suzuki-Miyaura couplings, and other boron-mediated transformations. Our product is rigorously tested to ensure ≥95% purity (GC) and is supplied in sealed containers under inert atmosphere to prevent degradation. Ideal for researchers requiring precise stoichiometry in catalytic systems or polymer modification studies.

Properties

• CAS Number: 23894-82-8
• Complexity: 103
• InChI: InChI=1S/C6H12BO2/c1-5-4-6(2,3)9-7-8-5/h5H,4H2,1-3H3
• InChI Key: KZAMKXKKAYRGLP-UHFFFAOYSA-N
• Exact Mass: 127.0930348
• Molecular Formula: C6H12BO2
• Molecular Weight: 126.97
• SMILES: [B]1OC(CC(O1)(C)C)C
• Topological: 18.5
• Monoisotopic Mass: 127.0930348
• Synonyms: 4,4,6-trimethyl-1,3,2-dioxaborinane, 23894-82-8, methyl pentane diol borane, SCHEMBL1014386, SCHEMBL4299249, ARSUQHZDPBOKDP-UHFFFAOYSA-N, DB-152976

Application

4,4,6-Trimethyl-1,3,2-dioxaborinane serves as a versatile reagent in transition-metal-catalyzed borylation reactions for aryl functionalization. It demonstrates particular utility in the synthesis of boron-doped organic semiconductors and luminescent materials. The compound’s sterically hindered structure makes it valuable for controlled radical polymerization processes. Researchers also employ it as a protected boronic acid equivalent in multistep synthetic routes.

If you are interested or have any questions, please contact us at support@atomfair.com

Disclaimer: Sold exclusively for laboratory research. Prohibited for commercial use, diagnostics, or human/animal applications. Buyers assume all compliance liability.