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CAS 857934-82-8

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2-(2-iodophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Description:
2-(2-Iodophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is an organoboron compound characterized by its unique boron-containing dioxaborolane ring structure. This compound features a phenyl group substituted with an iodine atom, which contributes to its reactivity and potential applications in organic synthesis, particularly in cross-coupling reactions. The presence of the tetramethyl substituents enhances its solubility and stability, making it suitable for various chemical processes. The dioxaborolane moiety is known for its ability to participate in nucleophilic reactions, and the iodine atom can serve as a leaving group in reactions such as Suzuki coupling. Additionally, this compound may exhibit interesting electronic properties due to the interplay between the iodine substituent and the boron atom, which can influence its reactivity and interaction with other molecules. Overall, 2-(2-iodophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a versatile compound with potential applications in medicinal chemistry and materials science.
Formula:C12H16BIO2
InChI:InChI=1/C12H16BIO2/c1-11(2)12(3,4)16-13(15-11)9-7-5-6-8-10(9)14/h5-8H,1-4H3
SMILES:CC1(C)C(C)(C)OB(c2ccccc2I)O1
Synonyms:
  • 1,3,2-Dioxaborolane, 2-(2-Iodophenyl)-4,4,5,5-Tetramethyl-
  • 2-(2-Iodophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
  • 2-Iodophenylboronic Acid Pinacol Ester
  • 1-Iodo-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene
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