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CAS 68716-49-4

:

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

Description:
2-(4-bromophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is an organoboron compound characterized by its unique dioxaborolane structure, which features a five-membered ring containing boron and oxygen atoms. This compound typically exhibits a high degree of stability due to the presence of the boron atom, which can participate in various chemical reactions, particularly in cross-coupling reactions in organic synthesis. The presence of the 4-bromophenyl group enhances its reactivity and solubility in organic solvents, making it useful in synthetic applications. The tetramethyl substituents contribute to steric hindrance, which can influence the compound's reactivity and interaction with other molecules. Additionally, this compound may exhibit interesting optical properties and can be utilized in the development of materials for organic electronics or as intermediates in the synthesis of pharmaceuticals. Its specific applications often depend on the functionalization of the boron atom and the overall molecular architecture, which can be tailored for desired chemical properties.
Formula:C12H16BBrO2
InChI:InChI=1/C12H16BBrO2/c1-11(2)12(3,4)16-13(15-11)9-5-7-10(14)8-6-9/h5-8H,1-4H3
SMILES:CC1(C)C(C)(C)OB(c2ccc(cc2)Br)O1
Synonyms:
  • 4-Bromophenylboronic acid pinacol ester
  • 2-(4-Bromo-Phenyl)-4,4,5,5-Tetramethyl-[1,3,2]Dioxaborolane
  • 1-Bromo-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene
  • 1,3,2-Dioxaborolane, 2-(4-bromophenyl)-4,4,5,5-tetramethyl-
  • 2-(4-Bromophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane &gt
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