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CAS 957061-22-2

:

B-[3-[[(3-Methoxypropyl)amino]carbonyl]phenyl]boronic acid

Description:
B-[3-[[(3-Methoxypropyl)amino]carbonyl]phenyl]boronic acid, with the CAS number 957061-22-2, is a boronic acid derivative characterized by the presence of a boron atom bonded to a phenyl group and an amino acid moiety. 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 drug development and materials science. The methoxypropyl group enhances its solubility in organic solvents, while the amino and carbonyl functionalities contribute to its reactivity and potential biological activity. Boronic acids are known for their role in Suzuki coupling reactions, which are essential in organic synthesis for forming carbon-carbon bonds. Additionally, this compound may exhibit specific interactions with biological targets, making it of interest in medicinal chemistry. Its structural features suggest potential applications in the development of therapeutic agents or as a tool in chemical biology.
Formula:C11H16BNO4
InChI:InChI=1S/C11H16BNO4/c1-17-7-3-6-13-11(14)9-4-2-5-10(8-9)12(15)16/h2,4-5,8,15-16H,3,6-7H2,1H3,(H,13,14)
InChI key:InChIKey=MICYHWLTBQBPRM-UHFFFAOYSA-N
SMILES:C(NCCCOC)(=O)C1=CC(B(O)O)=CC=C1
Synonyms:
  • (3-((3-Methoxypropyl)carbamoyl)phenyl)boronic acid
  • 3-(3-Methoxypropylcarbamoyl)phenylboronic acid
  • B-[3-[[(3-Methoxypropyl)amino]carbonyl]phenyl]boronic acid
  • Boronic acid, B-[3-[[(3-methoxypropyl)amino]carbonyl]phenyl]-
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