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CAS 871125-71-2

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B-(2,3,5,6-Tetrafluoro-4-propoxyphenyl)boronic acid

Description:
B-(2,3,5,6-Tetrafluoro-4-propoxyphenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is heavily substituted with fluorine and a propoxy group. The fluorine atoms contribute to the compound's unique electronic properties, enhancing its reactivity and potential applications in organic synthesis and materials science. The propoxy group provides solubility in organic solvents, making it useful in various chemical reactions, including Suzuki coupling reactions, which are pivotal in forming carbon-carbon bonds. This compound is likely to exhibit moderate stability under ambient conditions but may be sensitive to moisture due to the boronic acid moiety. Its structure suggests potential applications in pharmaceuticals, agrochemicals, and as a building block in the synthesis of more complex molecules. Additionally, the presence of multiple fluorine atoms can impart unique physical properties, such as increased lipophilicity and altered melting and boiling points compared to non-fluorinated analogs.
Formula:C9H9BF4O3
InChI:InChI=1S/C9H9BF4O3/c1-2-3-17-9-7(13)5(11)4(10(15)16)6(12)8(9)14/h15-16H,2-3H2,1H3
InChI key:InChIKey=IDDYYTHVGIJBNA-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(F)C(F)=C(OCCC)C(F)=C1F
Synonyms:
  • Boronic acid, B-(2,3,5,6-tetrafluoro-4-propoxyphenyl)-
  • B-(2,3,5,6-Tetrafluoro-4-propoxyphenyl)boronic acid
  • (2,3,5,6-Tetrafluoro-4-propoxyphenyl)boronic acid
  • (2,3,5,6-Tetrafluoro-4-propoxyphenyl)boronicacid
  • Boronic acid, (2,3,5,6-tetrafluoro-4-propoxyphenyl)-
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