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CAS 1451390-95-6

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

Description:
B-[2,4-Difluoro-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 at the 2 and 4 positions, enhancing its electronic properties and potentially influencing its reactivity. The presence of the 1-methylethoxy group contributes to its solubility and steric properties, which can affect its interaction with biological targets or other chemical species. This compound is typically used in cross-coupling reactions, such as Suzuki-Miyaura coupling, to form carbon-carbon bonds, and may also exhibit interesting biological activities due to its structural characteristics. As with many boronic acids, it is important to handle this substance with care, considering its potential reactivity and the need for appropriate storage conditions to maintain stability.
Formula:C9H11BF2O3
InChI:InChI=1S/C9H11BF2O3/c1-5(2)15-9-7(11)4-3-6(8(9)12)10(13)14/h3-5,13-14H,1-2H3
InChI key:InChIKey=LTXLJWCQTYVYCS-UHFFFAOYSA-N
SMILES:O(C(C)C)C1=C(F)C(B(O)O)=CC=C1F
Synonyms:
  • Boronic acid, B-[2,4-difluoro-3-(1-methylethoxy)phenyl]-
  • B-[2,4-Difluoro-3-(1-methylethoxy)phenyl]boronic acid
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