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CAS 2096338-86-0

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B-[2-Bromo-4-(1-methylethyl)phenyl]boronic acid

Description:
B-[2-Bromo-4-(1-methylethyl)phenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols and is widely used in organic synthesis, particularly in Suzuki coupling reactions. The compound features a bromine atom and an isopropyl group attached to a phenyl ring, contributing to its unique reactivity and steric properties. The presence of the bromine atom enhances its electrophilic character, making it a suitable candidate for cross-coupling reactions. Additionally, the boronic acid moiety allows for the formation of stable complexes with various substrates, facilitating the synthesis of complex organic molecules. This compound is typically used in research and development within the fields of medicinal chemistry and materials science, where its reactivity can be harnessed for the construction of diverse chemical architectures. As with many organoboron compounds, it is essential to handle it with care, considering its potential reactivity and the need for appropriate safety measures in laboratory settings.
Formula:C9H12BBrO2
InChI:InChI=1S/C9H12BBrO2/c1-6(2)7-3-4-8(10(12)13)9(11)5-7/h3-6,12-13H,1-2H3
InChI key:InChIKey=YEHIZUUXYLXRNS-UHFFFAOYSA-N
SMILES:C(C)(C)C1=CC(Br)=C(B(O)O)C=C1
Synonyms:
  • Boronic acid, B-[2-bromo-4-(1-methylethyl)phenyl]-
  • B-[2-Bromo-4-(1-methylethyl)phenyl]boronic acid
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