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CAS 957120-53-5

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B-[3-(Aminocarbonyl)-5-chlorophenyl]boronic acid

Description:
B-[3-(Aminocarbonyl)-5-chlorophenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that has both an amino and a carbonyl substituent. This compound typically exhibits properties such as being a white to off-white solid, soluble in polar solvents like water and methanol, and having a moderate melting point. The boronic acid moiety allows for participation in various chemical reactions, particularly in Suzuki coupling reactions, making it valuable in organic synthesis and medicinal chemistry. The presence of the amino and carbonyl groups enhances its reactivity and potential biological activity, possibly contributing to its role in drug development. Additionally, this compound may exhibit properties such as pH sensitivity due to the boronic acid group, which can influence its behavior in biological systems. Overall, B-[3-(Aminocarbonyl)-5-chlorophenyl]boronic acid is a versatile compound with applications in synthetic chemistry and pharmaceuticals.
Formula:C7H7BClNO3
InChI:InChI=1S/C7H7BClNO3/c9-6-2-4(7(10)11)1-5(3-6)8(12)13/h1-3,12-13H,(H2,10,11)
InChI key:InChIKey=YFWFJKMZBNMWMC-UHFFFAOYSA-N
SMILES:B(O)(O)C1=CC(C(N)=O)=CC(Cl)=C1
Synonyms:
  • Boronic acid, B-[3-(aminocarbonyl)-5-chlorophenyl]-
  • 3-Carbamoyl-5-chlorophenylboronic acid
  • B-[3-(Aminocarbonyl)-5-chlorophenyl]boronic acid
  • 3-Borono-5-chlorobenzamide, 3-(Aminocarbonyl)-5-chlorobenzeneboronic acid
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