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CAS 100379-00-8

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2,6-Dimethylphenylboronic acid

Description:
2,6-Dimethylphenylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a dimethyl-substituted phenyl ring. Its molecular structure features a phenyl ring with two methyl groups located at the 2 and 6 positions, which influences its reactivity and solubility. This compound is typically a white to off-white solid and is soluble in polar organic solvents, making it useful in various chemical applications. It is known for its ability to form reversible covalent bonds with diols, which is a key feature in applications such as Suzuki coupling reactions in organic synthesis. Additionally, 2,6-Dimethylphenylboronic acid can serve as a ligand in coordination chemistry and is utilized in the development of sensors and materials for drug delivery. Safety precautions should be taken when handling this compound, as boronic acids can be irritants and may pose environmental hazards. Overall, its unique structural properties make it a valuable compound in both academic and industrial chemistry.
Formula:C8H11BO2
InChI:InChI=1S/C8H11BO2/c1-6-4-3-5-7(2)8(6)9(10)11/h3-5,10-11H,1-2H3
InChI key:InChIKey=ZXDTWWZIHJEZOG-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(C)C=CC=C1C
Synonyms:
  • (2,4-Dimethylphenyl)Boronic Acid
  • (3,5-Dimethylphenyl)Boronic Acid
  • 2,6-Dimethylboronic acid
  • 2,6-Dimethylphenylboric acid
  • 2,6-Dimethylphenylboronic acid
  • 2,6-Xyleneboronic acid
  • 2,6-Xylylboronic acid
  • B-(2,6-Dimethylphenyl)boronic acid
  • Boronic acid, (2,6-dimethylphenyl)-
  • Boronic acid, B-(2,6-dimethylphenyl)-
  • m-Xylene-2-boronic Acid
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