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CAS 1072952-14-7

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B-(2-Amino-4,5-difluorophenyl)boronic acid

Description:
B-(2-Amino-4,5-difluorophenyl)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 amino and difluoro groups. This compound typically exhibits properties such as being a solid at room temperature, with potential solubility in polar solvents due to the presence of the boronic acid moiety. The amino group can participate in hydrogen bonding, enhancing its reactivity and potential applications in medicinal chemistry and materials science. The difluorophenyl substituent may influence the electronic properties of the molecule, potentially affecting its reactivity and interactions with biological targets. Boronic acids are known for their ability to form reversible covalent bonds with diols, making them useful in various applications, including drug development and as building blocks in organic synthesis. Overall, B-(2-Amino-4,5-difluorophenyl)boronic acid is a versatile compound with significant implications in chemical research and development.
Formula:C6H6BF2NO2
InChI:InChI=1S/C6H6BF2NO2/c8-4-1-3(7(11)12)6(10)2-5(4)9/h1-2,11-12H,10H2
InChI key:InChIKey=YDTCINIFZJCMSN-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(N)C=C(F)C(F)=C1
Synonyms:
  • Boronic acid, B-(2-amino-4,5-difluorophenyl)-
  • (2-Amino-4,5-difluorophenyl)boronic acid
  • B-(2-Amino-4,5-difluorophenyl)boronic acid
  • 2-Amino-4,5-difluorophenylboronic acid
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