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CAS 1451392-12-3

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B-(2-Fluoro-6-methoxy-3-methylphenyl)boronic acid

Description:
B-(2-Fluoro-6-methoxy-3-methylphenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a substituted phenyl ring. The compound features a fluorine atom and a methoxy group on the aromatic ring, which can influence its reactivity and solubility. Boronic acids are known for their ability to form reversible complexes with diols, making them valuable in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. The presence of the fluorine atom may enhance the compound's electronic properties, potentially affecting its reactivity and interaction with biological targets. Additionally, the methoxy group can provide steric hindrance and influence the compound's overall polarity. This compound may find applications in medicinal chemistry and materials science due to its unique structural features and reactivity profile. As with many boronic acids, it is important to handle this substance with care, considering its potential reactivity and the need for proper storage conditions to maintain stability.
Formula:C8H10BFO3
InChI:InChI=1S/C8H10BFO3/c1-5-3-4-6(13-2)7(8(5)10)9(11)12/h3-4,11-12H,1-2H3
InChI key:InChIKey=RHODPGLYWAVVBN-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(OC)C=CC(C)=C1F
Synonyms:
  • (2-Fluoro-6-methoxy-3-methylphenyl)boronic acid
  • B-(2-Fluoro-6-methoxy-3-methylphenyl)boronic acid
  • Boronic acid, B-(2-fluoro-6-methoxy-3-methylphenyl)-
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