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Atomfair 1-(Tetrahydro-2H-pyran-2-YL)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-YL)-1H-imidazole C14H23BN2O3

Description 1-(Tetrahydro-2H-pyran-2-YL)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-YL)-1H-imidazole (CAS: 1040377-03-4) is a high-purity boronic ester derivative featuring a tetrahydro-2H-pyran-protected imidazole core. This compound, with the molecular formula C14H23BN2O3, is a valuable intermediate in organic synthesis and pharmaceutical research. Its IUPAC name is 1-(oxan-2-yl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)imidazole . The pinacol boronate ester group enhances stability and reactivity, making it ideal for Suzuki-Miyaura cross-coupling reactions. This product is rigorously tested for quality, ensuring optimal performance in synthetic applications. Suitable for researchers and scientists requiring precise and reliable reagents.

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Description

Description

1-(Tetrahydro-2H-pyran-2-YL)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-YL)-1H-imidazole (CAS: 1040377-03-4) is a high-purity boronic ester derivative featuring a tetrahydro-2H-pyran-protected imidazole core. This compound, with the molecular formula C14H23BN2O3, is a valuable intermediate in organic synthesis and pharmaceutical research. Its IUPAC name is 1-(oxan-2-yl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)imidazole. The pinacol boronate ester group enhances stability and reactivity, making it ideal for Suzuki-Miyaura cross-coupling reactions. This product is rigorously tested for quality, ensuring optimal performance in synthetic applications. Suitable for researchers and scientists requiring precise and reliable reagents.

  • CAS No: 1040377-03-4
  • Molecular Formula: C14H23BN2O3
  • Molecular Weight: 278.16
  • Exact Mass: 278.1801728
  • Monoisotopic Mass: 278.1801728
  • IUPAC Name: 1-(oxan-2-yl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)imidazole
  • SMILES: B1(OC(C(O1)(C)C)(C)C)C2=CN=CN2C3CCCCO3
  • Synonyms: 1029684-37-4, 1-(TETRAHYDRO-2H-PYRAN-2-YL)-5-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)-1H-IMIDAZOLE, 1-(TETRAHYDRO-2H-PYRAN-2-YL)-1H-IMIDAZOLE-5-BORONIC ACID PINACOL ESTER, 1-(oxan-2-yl)-5-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-imidazole, 1-(oxan-2-yl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)imidazole

Application

This compound is widely used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions to form biaryl compounds. The tetrahydro-2H-pyran (THP) protecting group enhances stability during synthetic transformations. Researchers also utilize it in the development of boron-containing heterocycles for medicinal chemistry.

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