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Atomfair Pinacolborane C6H12BO2

Description Pinacolborane (CAS 25015-63-8) is a highly versatile and reactive organoboron compound with the molecular formula C6H12BO2. This colorless to pale yellow liquid is widely recognized for its role as a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in organic synthesis. Its stable dioxaborolane structure, featuring a boron atom coordinated within a pinacol framework, ensures excellent handling and storage stability under inert conditions. Pinacolborane is particularly valued for its ability to transfer boron groups to organic substrates, making it indispensable in pharmaceutical, agrochemical, and materials science research. Supplied in high purity (typically ??95%), it is…

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Description

Description

Pinacolborane (CAS 25015-63-8) is a highly versatile and reactive organoboron compound with the molecular formula C6H12BO2. This colorless to pale yellow liquid is widely recognized for its role as a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in organic synthesis. Its stable dioxaborolane structure, featuring a boron atom coordinated within a pinacol framework, ensures excellent handling and storage stability under inert conditions. Pinacolborane is particularly valued for its ability to transfer boron groups to organic substrates, making it indispensable in pharmaceutical, agrochemical, and materials science research. Supplied in high purity (typically ??95%), it is packaged under inert gas to maintain reactivity and shelf life. Suitable for use in anhydrous environments, this reagent is a must-have for synthetic chemists and researchers working on advanced boron chemistry applications.

  • CAS No: 25015-63-8
  • Molecular Formula: C6H12BO2
  • Molecular Weight: 126.97
  • Exact Mass: 127.0930348
  • Monoisotopic Mass: 127.0930348
  • SMILES: [B]1OC(C(O1)(C)C)(C)C
  • Synonyms: Pinacolborane, 4,4,5,5-Tetramethyl-1,3,2-dioxaborolane, 1,3,2-Dioxaborolane, 4,4,5,5-tetramethyl-, EC 607-485-3, DTXSID30422852

Application

Pinacolborane is extensively used in organic synthesis as a boron source for Suzuki-Miyaura cross-coupling reactions, facilitating the construction of biaryl compounds. It serves as a critical reagent in the preparation of boronic esters and acids, which are intermediates in drug discovery and material science. Additionally, its applications extend to catalytic borylation reactions and polymer chemistry, where it modifies molecular structures to achieve desired properties.

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