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CAS 352535-87-6

:

(5-chloro-2-fluoro-3-methylphenyl)boronic acid

Description:
(5-Chloro-2-fluoro-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 molecular structure features a phenyl ring with three substituents: a chlorine atom at the 5-position, a fluorine atom at the 2-position, and a methyl group at the 3-position. This compound is typically used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling, which is valuable for forming carbon-carbon bonds. The boronic acid group is known for its ability to form reversible complexes with diols, making it useful in various applications, including drug development and materials science. The presence of halogen substituents can influence the reactivity and solubility of the compound, while the methyl group can affect steric hindrance and electronic properties. Overall, (5-chloro-2-fluoro-3-methylphenyl)boronic acid is a versatile building block in synthetic organic chemistry.
Formula:C7H7BClFO2
InChI:InChI=1/C7H7BClFO2/c1-4-2-5(9)3-6(7(4)10)8(11)12/h2-3,11-12H,1H3
SMILES:Cc1cc(cc(c1F)B(O)O)Cl
Synonyms:
  • boronic acid, B-(5-chloro-2-fluoro-3-methylphenyl)-
  • (5-Chloro-2-fluoro-3-methylphenyl)boronic acid
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