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CAS 330793-46-9

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B-[4-[[(2-Phenylethyl)amino]carbonyl]phenyl]boronic acid

Description:
B-[4-[[(2-Phenylethyl)amino]carbonyl]phenyl]boronic acid, identified by its CAS number 330793-46-9, 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 features a phenyl ring substituted with a carbonyl group linked to a 2-phenylethylamino group, which contributes to its potential biological activity. Boronic acids are known for their ability to form reversible covalent bonds with diols, making them valuable in various applications, including drug development and molecular recognition. The presence of the amino group suggests potential interactions with biological targets, enhancing its relevance in medicinal chemistry. Additionally, the compound's structural features may influence its solubility, stability, and reactivity, which are critical for its application in synthetic and pharmaceutical chemistry. Overall, this compound exemplifies the diverse functionalities that can be achieved through boronic acid chemistry, particularly in the context of drug design and development.
Formula:C15H16BNO3
InChI:InChI=1S/C15H16BNO3/c18-15(13-6-8-14(9-7-13)16(19)20)17-11-10-12-4-2-1-3-5-12/h1-9,19-20H,10-11H2,(H,17,18)
InChI key:InChIKey=VTXXKSNJPIRHMK-UHFFFAOYSA-N
SMILES:C(NCCC1=CC=CC=C1)(=O)C2=CC=C(B(O)O)C=C2
Synonyms:
  • (4-(Phenethylcarbamoyl)phenyl)boronic acid
  • B-[4-[[(2-Phenylethyl)amino]carbonyl]phenyl]boronic acid
  • Boronic acid, B-[4-[[(2-phenylethyl)amino]carbonyl]phenyl]-
  • (4-(Phenethylcarbamoyl)phenyl)boronicacid
  • Boronic acid, [4-[[(2-phenylethyl)amino]carbonyl]phenyl]-
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