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CAS 871126-28-2

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B-[2,3,5,6-Tetrafluoro-4-(1-methylethoxy)phenyl]boronic acid

Description:
B-[2,3,5,6-Tetrafluoro-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 four fluorine atoms and an ethoxy group, which enhances its reactivity and solubility in organic solvents. The presence of fluorine atoms typically imparts unique electronic properties, such as increased lipophilicity and altered reactivity, which can be advantageous in drug design. Additionally, boronic acids are often utilized in cross-coupling reactions, such as Suzuki-Miyaura coupling, to form carbon-carbon bonds. The specific structure of this compound suggests potential applications in the development of pharmaceuticals or agrochemicals, where selective reactivity and stability are crucial. Overall, B-[2,3,5,6-Tetrafluoro-4-(1-methylethoxy)phenyl]boronic acid exemplifies the versatility of boron-containing compounds in modern chemistry.
Formula:C9H9BF4O3
InChI:InChI=1/C9H9BF4O3/c1-3(2)17-9-7(13)5(11)4(10(15)16)6(12)8(9)14/h3,15-16H,1-2H3
InChI key:InChIKey=YOXGBYWSEKQTAW-UHFFFAOYSA-N
SMILES:O(C(C)C)C1=C(F)C(F)=C(B(O)O)C(F)=C1F
Synonyms:
  • [2,3,5,6-Tetrafluoro-4-(propan-2-yloxy)phenyl]boronic acid
  • B-[2,3,5,6-Tetrafluoro-4-(1-methylethoxy)phenyl]boronic acid
  • Boronic acid, [2,3,5,6-tetrafluoro-4-(1-methylethoxy)phenyl]-
  • (2,3,5,6-Tetrafluoro-4-isopropoxyphenyl)boronicacid
  • Boronic acid, B-[2,3,5,6-tetrafluoro-4-(1-methylethoxy)phenyl]-
  • [2,3,5,6-TETRAFLUORO-4-(1-METHYLETHOXY)PHENYL]BORONIC ACID
  • (2,3,5,6-Tetrafluoro-4-isopropoxyphenyl)-boronic acid
  • (2,3,5,6-tetrafluoro-4-propan-2-yloxyphenyl)boronic acid
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