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CAS 130870-00-7

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4-Bromo-2,5-dimethylphenylboronic acid

Description:
4-Bromo-2,5-dimethylphenylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is further substituted with bromine and methyl groups. This compound typically exhibits a white to off-white crystalline appearance and is soluble in polar solvents such as water and alcohols, which is a characteristic feature of boronic acids due to their ability to form hydrogen bonds. The presence of the bromine atom and methyl groups influences its reactivity and stability, making it useful in various chemical reactions, particularly in Suzuki coupling reactions for the formation of carbon-carbon bonds. Additionally, boronic acids are known for their ability to form reversible complexes with diols, which can be exploited in sensing applications. The compound's molecular structure contributes to its potential applications in organic synthesis, medicinal chemistry, and materials science. Safety precautions should be taken when handling this substance, as with many organoboron compounds, due to potential toxicity and environmental concerns.
Formula:C8H10BBrO2
InChI:InChI=1/C8H10BBrO2/c1-5-4-8(10)6(2)3-7(5)9(11)12/h3-4,11-12H,1-2H3
SMILES:Cc1cc(c(C)cc1B(O)O)Br
Synonyms:
  • Akos Brn-0722
  • 4-Bromo-2,5-Dimethylphenylboro
  • (4-Bromo-2,5-dimethyphenyl)boronic acid
  • 4-Bromo-2,5-dimethylbenzeneboronic acid
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