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CAS 2096337-66-3

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B-[2,6-Difluoro-4-(1-methylethoxy)phenyl]boronic acid

Description:
B-[2,6-Difluoro-4-(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 6 positions, enhancing its electronic properties and potentially influencing its reactivity. The presence of a 1-methylethoxy group at the para position (4-position) provides steric hindrance and may affect solubility and interaction with biological targets. This compound is likely to exhibit moderate to high polarity due to the boronic acid group and the ether functionality, which can influence its behavior in different solvents. Additionally, boronic acids are often utilized in cross-coupling reactions, making this compound potentially valuable in the synthesis of complex organic molecules. Its specific properties, such as melting point, solubility, and reactivity, would need to be determined through experimental methods.
Formula:C9H11BF2O3
InChI:InChI=1S/C9H11BF2O3/c1-5(2)15-6-3-7(11)9(10(13)14)8(12)4-6/h3-5,13-14H,1-2H3
InChI key:InChIKey=DHCDNEJEXMOLHK-UHFFFAOYSA-N
SMILES:O(C(C)C)C1=CC(F)=C(B(O)O)C(F)=C1
Synonyms:
  • Boronic acid, B-[2,6-difluoro-4-(1-methylethoxy)phenyl]-
  • B-[2,6-Difluoro-4-(1-methylethoxy)phenyl]boronic acid
  • 2,6-Difluoro-4-isopropoxyphenylboronic acid
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