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CAS 408492-26-2

:

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

Description:
2-(3,5-Dibromophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is an organoboron compound characterized by its unique dioxaborolane structure, which features a boron atom bonded to two oxygen atoms in a cyclic arrangement. This compound contains a dibromophenyl group, contributing to its potential reactivity and applications in organic synthesis, particularly in cross-coupling reactions. The presence of the tetramethyl substituents enhances its stability and solubility in organic solvents. Typically, compounds like this exhibit moderate to high thermal stability, making them suitable for various chemical transformations. The dibromophenyl moiety can serve as a versatile building block in the synthesis of more complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, the boron atom can participate in various reactions, such as nucleophilic substitutions and the formation of organometallic complexes. Overall, this compound is of interest in both academic research and industrial applications due to its functional groups and structural features that facilitate diverse chemical reactions.
Formula:C12H15BBr2O2
InChI:InChI=1S/C12H15BBr2O2/c1-11(2)12(3,4)17-13(16-11)8-5-9(14)7-10(15)6-8/h5-7H,1-4H3
InChI key:InChIKey=WJYKUCWENIHKOC-UHFFFAOYSA-N
SMILES:CC1(C)OB(OC1(C)C)C2=CC(Br)=CC(Br)=C2
Synonyms:
  • 1,3,2-Dioxaborolane, 2-(3,5-dibromophenyl)-4,4,5,5-tetramethyl-
  • 1,3-Dibromo-5-(pinacolboryl)benzene
  • 2-(3,5-Dibromophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
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