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CAS 957060-72-9

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Boronic acid, B-[4-[[[2-(1-piperidinyl)ethyl]amino]carbonyl]phenyl]-, hydrochloride (1:1)

Description:
Boronic acid, specifically the compound with the name "B-[4-[[[2-(1-piperidinyl)ethyl]amino]carbonyl]phenyl]-, hydrochloride (1:1)" and CAS number 957060-72-9, is characterized by its boronic acid functional group, which typically exhibits properties such as the ability to form reversible covalent bonds with diols, making it useful in various chemical applications, including drug development and organic synthesis. This compound features a piperidine moiety, which contributes to its biological activity and solubility characteristics. The hydrochloride form indicates that it is a salt, enhancing its stability and solubility in aqueous solutions. Boronic acids are known for their role in Suzuki coupling reactions, a key method in organic chemistry for forming carbon-carbon bonds. Additionally, the presence of the amino and carbonyl groups suggests potential interactions with biological targets, making this compound of interest in medicinal chemistry. Overall, its unique structural features and functional groups position it as a versatile compound in both synthetic and pharmaceutical chemistry.
Formula:C14H22BClN2O3
InChI:InChI=1S/C14H21BN2O3.ClH/c18-14(12-4-6-13(7-5-12)15(19)20)16-8-11-17-9-2-1-3-10-17;/h4-7,19-20H,1-3,8-11H2,(H,16,18);1H
InChI key:InChIKey=WEPTXOJQSHKUJD-UHFFFAOYSA-N
SMILES:C(NCCN1CCCCC1)(=O)C2=CC=C(B(O)O)C=C2.Cl
Synonyms:
  • Boronic acid, B-[4-[[[2-(1-piperidinyl)ethyl]amino]carbonyl]phenyl]-, hydrochloride (1:1)
  • 4-{[2-(Piperidin-1-yl)ethyl]carbamoyl}benzeneboronicacidhydrochloride98%
  • [4-(2-piperidin-1-ylethylcarbamoyl)phenyl]boronic acid
  • 4-[2-(1-Piperidino)ethylcarbamoyl]benzeneboronic acid hydrochloride, 98%
  • 4-Borono-N-[2-(piperidin-1-yl)ethyl]benzamide hydrochloride
  • (4-((2-(Piperidin-1-yl)ethyl)carbaMoyl)phenyl)boronic acid hydrochloride
  • 4-[2-(1-Piperidinyl)ethylcarbaMoyl]benzeneboronic acid hydrochloride, 98%
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