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Atomfair Diisopropyl Allylboronate C9H19BO2

Description Diisopropyl Allylboronate (CAS No. 51851-79-7) is a highly versatile organoboron compound with the molecular formula C9H19BO2. This reagent is widely utilized in organic synthesis, particularly in allylation reactions, due to its stability and reactivity under mild conditions. The IUPAC name, di(propan-2-yloxy)-prop-2-enylborane , reflects its structural composition, featuring an allyl group bonded to a boronate ester. This compound is typically supplied as a clear, colorless to pale yellow liquid with high purity (>95%) and is stored under inert conditions to prevent degradation. Ideal for researchers and chemists, Diisopropyl Allylboronate is a critical building block for the synthesis of complex molecules,…

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Description

Description

Diisopropyl Allylboronate (CAS No. 51851-79-7) is a highly versatile organoboron compound with the molecular formula C9H19BO2. This reagent is widely utilized in organic synthesis, particularly in allylation reactions, due to its stability and reactivity under mild conditions. The IUPAC name, di(propan-2-yloxy)-prop-2-enylborane, reflects its structural composition, featuring an allyl group bonded to a boronate ester. This compound is typically supplied as a clear, colorless to pale yellow liquid with high purity (>95%) and is stored under inert conditions to prevent degradation. Ideal for researchers and chemists, Diisopropyl Allylboronate is a critical building block for the synthesis of complex molecules, including pharmaceuticals, agrochemicals, and advanced materials.

  • CAS No: 51851-79-7
  • Molecular Formula: C9H19BO2
  • Molecular Weight: 170.06
  • Exact Mass: 170.1478100
  • Monoisotopic Mass: 170.1478100
  • IUPAC Name: di(propan-2-yloxy)-prop-2-enylborane
  • SMILES: B(CC=C)(OC(C)C)OC(C)C
  • Synonyms: Diisopropyl Allylboronate, 51851-79-7, DTXSID60465712, DTXCID50416531, 679-763-2

Application

Diisopropyl Allylboronate is extensively used in organic synthesis for the allylation of carbonyl compounds, enabling the formation of homoallylic alcohols with high stereoselectivity. It serves as a key intermediate in the preparation of chiral compounds, particularly in asymmetric synthesis and medicinal chemistry. Researchers also employ this reagent in cross-coupling reactions and the construction of carbon-carbon bonds under mild conditions.

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