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CAS 2096339-90-9

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B-[2,4-Difluoro-5-methyl-3-(1-methylethoxy)phenyl]boronic acid

Description:
B-[2,4-Difluoro-5-methyl-3-(1-methylethoxy)phenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The compound features a phenyl ring substituted with two fluorine atoms and a methyl group, contributing to its unique electronic properties and potential reactivity. The presence of the 1-methylethoxy group enhances its solubility and stability in organic solvents. This compound may exhibit interesting biological activity due to its structural features, making it a candidate for further research in drug development or as a reagent in cross-coupling reactions. Its specific characteristics, such as melting point, solubility, and reactivity, would depend on the molecular interactions and the environment in which it is used. As with many boronic acids, it is important to handle this compound with care, considering its potential reactivity and the need for proper storage conditions.
Formula:C10H13BF2O3
InChI:InChI=1S/C10H13BF2O3/c1-5(2)16-10-8(12)6(3)4-7(9(10)13)11(14)15/h4-5,14-15H,1-3H3
InChI key:InChIKey=CJYRRWCWAJPESW-UHFFFAOYSA-N
SMILES:O(C(C)C)C1=C(F)C(B(O)O)=CC(C)=C1F
Synonyms:
  • Boronic acid, B-[2,4-difluoro-5-methyl-3-(1-methylethoxy)phenyl]-
  • B-[2,4-Difluoro-5-methyl-3-(1-methylethoxy)phenyl]boronic acid
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