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CAS 1072945-88-0

:

B-[1-(3-Chlorophenyl)-1H-pyrazol-4-yl]boronic acid

Description:
B-[1-(3-Chlorophenyl)-1H-pyrazol-4-yl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a pyrazole ring, which is further substituted with a chlorophenyl group. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The presence of the chlorophenyl moiety can influence its electronic properties and reactivity, potentially enhancing its biological activity. Additionally, boronic acids are known for their role in Suzuki coupling reactions, which are pivotal in the formation of carbon-carbon bonds in organic synthesis. The compound's structure suggests potential applications in drug development, particularly in targeting specific biological pathways. Its solubility and stability in various solvents can vary, which is important for its practical applications in laboratory settings. Overall, B-[1-(3-Chlorophenyl)-1H-pyrazol-4-yl]boronic acid represents a versatile building block in synthetic organic chemistry.
Formula:C9H8BClN2O2
InChI:InChI=1S/C9H8BClN2O2/c11-8-2-1-3-9(4-8)13-6-7(5-12-13)10(14)15/h1-6,14-15H
InChI key:InChIKey=QQIIJLJSZUIAKB-UHFFFAOYSA-N
SMILES:B(O)(O)C1=CN(N=C1)C2=CC(Cl)=CC=C2
Synonyms:
  • Boronic acid, B-[1-(3-chlorophenyl)-1H-pyrazol-4-yl]-
  • B-[1-(3-Chlorophenyl)-1H-pyrazol-4-yl]boronic acid
  • 1-(3-Chlorophenyl)pyrazole-4-boronic acid
  • [1-(3-Chlorophenyl)-1H-pyrazol-4-yl]boronic acid
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