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CAS 957061-04-0

:

B-[3-Chloro-2-(4-morpholinyl)-4-pyridinyl]boronic acid

Description:
B-[3-Chloro-2-(4-morpholinyl)-4-pyridinyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols and other nucleophiles. This compound features a pyridine ring substituted with a chlorine atom and a morpholine group, contributing to its potential biological activity and solubility properties. The boronic acid moiety is significant in medicinal chemistry, particularly in the development of inhibitors for various enzymes, including proteasomes and kinases. The presence of the morpholine ring enhances the compound's lipophilicity and may improve its pharmacokinetic properties. Additionally, the chlorine substituent can influence the electronic properties of the molecule, potentially affecting its reactivity and interaction with biological targets. Overall, this compound's unique structural features make it a valuable candidate for research in drug development and chemical biology.
Formula:C9H12BClN2O3
InChI:InChI=1S/C9H12BClN2O3/c11-8-7(10(14)15)1-2-12-9(8)13-3-5-16-6-4-13/h1-2,14-15H,3-6H2
InChI key:InChIKey=NCQGXSBDQBKPEJ-UHFFFAOYSA-N
SMILES:ClC1=C(N=CC=C1B(O)O)N2CCOCC2
Synonyms:
  • (3-Chloro-2-morpholinopyridin-4-yl)boronic acid
  • (3-Chloro-2-morpholinopyridin-4-yl)boronicacid
  • 3-Chloro-2-morpholinopyridine-4-boronic acid
  • B-[3-Chloro-2-(4-morpholinyl)-4-pyridinyl]boronic acid
  • [3-Chloro-2-(morpholin-4-yl)pyridin-4-yl]boronic acid
  • boronic acid, B-[3-chloro-2-(4-morpholinyl)-4-pyridinyl]-
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