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CAS 897958-93-9

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(2,5-difluoro-4-methoxyphenyl)boronic acid

Description:
(2,5-Difluoro-4-methoxyphenyl)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 two fluorine atoms at the 2 and 5 positions and a methoxy group at the 4 position of the aromatic ring, which influences its electronic properties and reactivity. Boronic acids are known for their ability to form reversible covalent bonds with diols, making them valuable in organic synthesis and medicinal chemistry, particularly in the development of pharmaceuticals and agrochemicals. This compound is typically a white to off-white solid and is soluble in polar organic solvents. Its unique structure allows it to participate in various chemical reactions, including Suzuki coupling, which is widely used for the formation of carbon-carbon bonds. Additionally, the presence of fluorine atoms can enhance the compound's lipophilicity and biological activity, making it of interest in drug design and development. Safety and handling precautions should be observed, as with all chemical substances, to mitigate any potential hazards.
Formula:C7H7BF2O3
InChI:InChI=1/C7H7BF2O3/c1-13-7-3-5(9)4(8(11)12)2-6(7)10/h2-3,11-12H,1H3
SMILES:COc1cc(c(cc1F)B(O)O)F
Synonyms:
  • boronic acid, B-(2,5-difluoro-4-methoxyphenyl)-
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