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CAS 957120-59-1

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B-[3-Chloro-5-[(diethylamino)carbonyl]phenyl]boronic acid

Description:
B-[3-Chloro-5-[(diethylamino)carbonyl]phenyl]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 is widely used in organic synthesis and medicinal chemistry. The compound features a chlorinated phenyl ring, which can enhance its reactivity and solubility in various solvents. The diethylamino group contributes to its basicity and can influence the compound's interaction with biological targets. This substance is typically utilized in the development of pharmaceuticals, particularly in the synthesis of compounds that inhibit specific enzymes or receptors. Its boronic acid moiety allows for participation in Suzuki-Miyaura cross-coupling reactions, making it valuable in the construction of complex organic molecules. Additionally, the presence of the carbonyl group adjacent to the diethylamino moiety may affect the compound's electronic properties and stability. Overall, this compound exemplifies the versatility of boronic acids in synthetic chemistry and drug development.
Formula:C11H15BClNO3
InChI:InChI=1S/C11H15BClNO3/c1-3-14(4-2)11(15)8-5-9(12(16)17)7-10(13)6-8/h5-7,16-17H,3-4H2,1-2H3
InChI key:InChIKey=KVYOLHXPKSCLCF-UHFFFAOYSA-N
SMILES:C(N(CC)CC)(=O)C1=CC(B(O)O)=CC(Cl)=C1
Synonyms:
  • 3-Chloro-5-(diethylcarbamoyl)phenylboronic acid
  • B-[3-Chloro-5-[(diethylamino)carbonyl]phenyl]boronic acid
  • N-Diethyl 3-borono-5-chlorobenzamide
  • Boronic acid, B-[3-chloro-5-[(diethylamino)carbonyl]phenyl]-
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