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CAS 476004-83-8

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2,2′-(2,5-Furandiyl)bis[4,4,5,5-tetramethyl-1,3,2-dioxaborolane]

Description:
2,2′-(2,5-Furandiyl)bis[4,4,5,5-tetramethyl-1,3,2-dioxaborolane] is an organoboron compound characterized by its unique structure, which includes two boron-containing dioxaborolane units linked by a furan moiety. This compound typically exhibits a high degree of stability due to the presence of the boron atoms, which can participate in various chemical reactions, including cross-coupling reactions, making it valuable in organic synthesis and materials science. The dioxaborolane groups contribute to its solubility in organic solvents and its potential as a reagent in Suzuki coupling reactions. Additionally, the furan ring adds to its aromatic character, potentially influencing its electronic properties and reactivity. The compound is likely to be a colorless to pale yellow solid, and its handling requires standard laboratory safety precautions due to the presence of boron and organic components. Overall, this compound represents a versatile building block in the development of advanced materials and pharmaceuticals.
Formula:C16H26B2O5
InChI:InChI=1S/C16H26B2O5/c1-13(2)14(3,4)21-17(20-13)11-9-10-12(19-11)18-22-15(5,6)16(7,8)23-18/h9-10H,1-8H3
InChI key:InChIKey=FOQCCZCSUIHXCG-UHFFFAOYSA-N
SMILES:CC1(C)OB(OC1(C)C)C=2OC(=CC2)B3OC(C)(C)C(C)(C)O3
Synonyms:
  • 1,3,2-Dioxaborolane, 2,2′-(2,5-furandiyl)bis[4,4,5,5-tetramethyl-
  • 2,5-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)furan
  • 2,2′-(2,5-Furandiyl)bis[4,4,5,5-tetramethyl-1,3,2-dioxaborolane]
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