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CAS 1218790-34-1

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2-[3-Bromo-5-(1-methylethoxy)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Description:
2-[3-Bromo-5-(1-methylethoxy)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a boron-containing organic compound characterized by its unique structural features, including a dioxaborolane ring and a brominated phenyl group. The presence of the bromine atom enhances its reactivity, making it useful in various synthetic applications, particularly in cross-coupling reactions such as Suzuki coupling. The tetramethyl substituents on the dioxaborolane ring contribute to its stability and solubility in organic solvents. This compound is typically used in organic synthesis and medicinal chemistry, where it may serve as an intermediate or a reagent. Its specific properties, such as melting point, boiling point, and solubility, can vary based on the purity and the conditions under which it is handled. As with many organoboron compounds, it is important to handle it with care, considering potential reactivity and toxicity. Overall, this compound exemplifies the versatility of boron chemistry in facilitating complex organic transformations.
Formula:C15H22BBrO3
InChI:InChI=1S/C15H22BBrO3/c1-10(2)18-13-8-11(7-12(17)9-13)16-19-14(3,4)15(5,6)20-16/h7-10H,1-6H3
InChI key:InChIKey=SDXSFUDLZJNXFE-UHFFFAOYSA-N
SMILES:CC1(C)OB(OC1(C)C)C2=CC(OC(C)C)=CC(Br)=C2
Synonyms:
  • 2-[3-Bromo-5-(1-methylethoxy)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
  • 1,3,2-Dioxaborolane, 2-[3-bromo-5-(1-methylethoxy)phenyl]-4,4,5,5-tetramethyl-
  • 3-Bromo-5-isopropoxyphenylboronic acid, pinacol ester
  • 2-(3-Bromo-5-isopropoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
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