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Atomfair 2,3,4,5,6-Pentafluorobenzeneboronic acid Pentafluorophenylboronic acid C6H2BF5O2
Description 2,3,4,5,6-Pentafluorobenzeneboronic acid (CAS No. 1582-24-7) is a highly fluorinated boronic acid derivative with the molecular formula C6H2BF5O2. This compound, also known as (2,3,4,5,6-pentafluorophenyl)boronic acid , is a valuable reagent in organic synthesis and materials science due to its electron-deficient aromatic ring and reactive boronic acid group. The pentafluorophenyl moiety enhances its stability and reactivity, making it ideal for Suzuki-Miyaura cross-coupling reactions, a cornerstone in the construction of complex biaryl structures. With a purity of ??95%, this product is rigorously tested by HPLC and NMR to ensure consistent quality for research and industrial applications. It is supplied as a white…
Description
Description
2,3,4,5,6-Pentafluorobenzeneboronic acid (CAS No. 1582-24-7) is a highly fluorinated boronic acid derivative with the molecular formula C6H2BF5O2. This compound, also known as (2,3,4,5,6-pentafluorophenyl)boronic acid, is a valuable reagent in organic synthesis and materials science due to its electron-deficient aromatic ring and reactive boronic acid group. The pentafluorophenyl moiety enhances its stability and reactivity, making it ideal for Suzuki-Miyaura cross-coupling reactions, a cornerstone in the construction of complex biaryl structures. With a purity of ??95%, this product is rigorously tested by HPLC and NMR to ensure consistent quality for research and industrial applications. It is supplied as a white to off-white crystalline powder, soluble in common organic solvents such as THF, DMF, and DMSO. Store under inert conditions at 2-8??C to maintain stability.
- CAS No: 1582-24-7
- Molecular Formula: C6H2BF5O2
- Molecular Weight: 211.88
- Exact Mass: 212.0068003
- Monoisotopic Mass: 212.0068003
- IUPAC Name: (2,3,4,5,6-pentafluorophenyl)boronic acid
- SMILES: B(C1=C(C(=C(C(=C1F)F)F)F)F)(O)O
- Synonyms: 2,3,4,5,6-PENTAFLUOROBENZENEBORONIC ACID, 627-867-3, 1582-24-7, Pentafluorophenylboronic acid, Perfluorophenylboronic acid
Application
2,3,4,5,6-Pentafluorobenzeneboronic acid is widely used in palladium-catalyzed cross-coupling reactions, particularly Suzuki-Miyaura couplings, to synthesize fluorinated biaryl compounds for pharmaceuticals and agrochemicals. Its electron-deficient aromatic ring facilitates reactions with aryl halides, enabling the creation of complex molecular architectures. This compound is also employed in the development of fluorescent probes and organic electronic materials due to its unique electronic properties. Researchers utilize it in the preparation of boron-containing polymers and covalent organic frameworks (COFs).
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