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CAS 156684-91-2

:

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

Description:
B-[2,3-Difluoro-4-(pentyloxy)phenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is substituted with both difluoro and pentyloxy groups. The difluoro substituents enhance the compound's electronic properties, potentially influencing its reactivity and interactions in various chemical environments. The pentyloxy group contributes to the hydrophobic character of the molecule, which may affect its solubility in organic solvents and its behavior in biological systems. Boronic acids are known for their ability to form reversible covalent bonds with diols, making them valuable in organic synthesis and materials science, particularly in the development of sensors and drug delivery systems. The specific structural features of this compound suggest potential applications in medicinal chemistry and materials development, where fine-tuning of electronic and steric properties is crucial. Overall, B-[2,3-Difluoro-4-(pentyloxy)phenyl]boronic acid exemplifies the versatility of boronic acids in various chemical applications.
Formula:C11H15BF2O3
InChI:InChI=1S/C11H15BF2O3/c1-2-3-4-7-17-9-6-5-8(12(15)16)10(13)11(9)14/h5-6,15-16H,2-4,7H2,1H3
InChI key:InChIKey=RCVQAXDDFSTKKQ-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(F)C(F)=C(OCCCCC)C=C1
Synonyms:
  • [2,3-Difluoro-4-(pentyloxy)phenyl]Boronic acid
  • B-[2,3-Difluoro-4-(pentyloxy)phenyl]boronic acid
  • Boronic acid, [2,3-difluoro-4-(pentyloxy)phenyl]-
  • Boronic acid, B-[2,3-difluoro-4-(pentyloxy)phenyl]-
  • 2,3-Difluoro-4-pentoxyphenylboronic acid
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