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CAS 352535-88-7

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Boronic acid, (3-chloro-2-fluoro-5-methylphenyl)-

Description:
Boronic acid, specifically (3-chloro-2-fluoro-5-methylphenyl)-, is an organoboron compound characterized by the presence of a boronic acid functional group (-B(OH)2) attached to a substituted aromatic ring. The compound features a phenyl ring that is modified with a chlorine atom at the 3-position, a fluorine atom at the 2-position, and a methyl group at the 5-position, contributing to its unique reactivity and properties. Boronic acids are known for their ability to form reversible complexes with diols, making them valuable in organic synthesis, particularly in the formation of carbon-carbon bonds through Suzuki coupling reactions. The presence of halogen substituents can influence the electronic properties of the molecule, affecting its reactivity and solubility. Additionally, boronic acids are often utilized in medicinal chemistry and materials science due to their versatile reactivity and ability to participate in various chemical transformations. Overall, this compound exemplifies the diverse applications of boronic acids in modern chemistry.
Formula:C7H7BClFO2
InChI:InChI=1S/C7H7BClFO2/c1-4-2-5(8(11)12)7(10)6(9)3-4/h2-3,11-12H,1H3
InChI key:InChIKey=BMTZFSDVTSWLLA-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(F)C(Cl)=CC(C)=C1
Synonyms:
  • Boronic acid, (3-chloro-2-fluoro-5-methylphenyl)-
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