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CAS 942070-06-6

:

2-(4-Bromo-2-thienyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Description:
2-(4-Bromo-2-thienyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is an organoboron compound characterized by its unique structural features, including a dioxaborolane ring and a thienyl group substituted with a bromine atom. The presence of the dioxaborolane moiety imparts significant reactivity, particularly in cross-coupling reactions, making it valuable in organic synthesis and materials science. The bromine atom enhances the compound's electrophilicity, facilitating nucleophilic attack in various chemical transformations. Additionally, the tetramethyl substitution contributes to the compound's stability and solubility in organic solvents. This compound is typically used in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals, due to its ability to participate in Suzuki-Miyaura coupling reactions. Its unique properties make it a subject of interest in research focused on developing new synthetic methodologies and exploring its potential applications in various fields, including medicinal chemistry and materials development.
Formula:C10H14BBrO2S
InChI:InChI=1S/C10H14BBrO2S/c1-9(2)10(3,4)14-11(13-9)8-5-7(12)6-15-8/h5-6H,1-4H3
InChI key:InChIKey=XOLVNUOSAPZSLF-UHFFFAOYSA-N
SMILES:CC1(C)OB(OC1(C)C)C2=CC(Br)=CS2
Synonyms:
  • 2-(4-Bromo-2-thienyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
  • 1,3,2-Dioxaborolane, 2-(4-bromo-2-thienyl)-4,4,5,5-tetramethyl-
  • 4-Bromothiophene-2-boronic acid pinacol ester
  • 2-(4-Bromothiophen-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
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