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CAS 874459-76-4

:

B-[3-[(2-Methyl-1-oxopropyl)amino]phenyl]boronic acid

Description:
B-[3-[(2-Methyl-1-oxopropyl)amino]phenyl]boronic acid, with the CAS number 874459-76-4, is a boronic acid derivative characterized by the presence of a boron atom bonded to a phenyl group and an amino substituent. 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 amino group enhances its reactivity and potential for biological activity, as it can participate in hydrogen bonding and interact with biological targets. Additionally, the methyl and oxopropyl groups contribute to its steric and electronic properties, influencing its solubility and stability. Boronic acids are often utilized in the development of pharmaceuticals, particularly in the context of cancer treatment and as inhibitors of certain enzymes. Overall, this compound's unique structure and functional groups make it a valuable candidate for research in both synthetic and medicinal chemistry.
Formula:C10H14BNO3
InChI:InChI=1S/C10H14BNO3/c1-7(2)10(13)12-9-5-3-4-8(6-9)11(14)15/h3-7,14-15H,1-2H3,(H,12,13)
InChI key:InChIKey=HXBVOKMSEWLCKA-UHFFFAOYSA-N
SMILES:N(C(C(C)C)=O)C1=CC(B(O)O)=CC=C1
Synonyms:
  • 3-(Isobutanoylamino)benzeneboronic acid
  • 3-Isobutyrylaminophenylboronic acid
  • B-[3-[(2-Methyl-1-oxopropyl)amino]phenyl]boronic acid
  • Boronic acid, B-[3-[(2-methyl-1-oxopropyl)amino]phenyl]-
  • Boronic acid, [3-[(2-methyl-1-oxopropyl)amino]phenyl]-
  • [3-(Isobutanoylamino)phenyl]boronic acid
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