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CAS 874219-49-5

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B-[4-[(Methylphenylamino)carbonyl]phenyl]boronic acid

Description:
B-[4-[(Methylphenylamino)carbonyl]phenyl]boronic acid, identified by its CAS number 874219-49-5, 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. This compound features a phenyl ring substituted with a methylphenylamino group and a carbonyl moiety, contributing to its potential reactivity and solubility properties. Boronic acids are often utilized in organic synthesis, particularly in Suzuki coupling reactions, which are valuable for forming carbon-carbon bonds. The presence of the amino and carbonyl groups may enhance its biological activity, making it of interest in medicinal chemistry. Additionally, the compound's structural features suggest potential applications in materials science and catalysis. Its solubility in organic solvents and stability under various conditions are also important characteristics that influence its practical applications. Overall, B-[4-[(Methylphenylamino)carbonyl]phenyl]boronic acid represents a versatile compound with significant implications in both synthetic and applied chemistry.
Formula:C14H14BNO3
InChI:InChI=1S/C14H14BNO3/c1-16(13-5-3-2-4-6-13)14(17)11-7-9-12(10-8-11)15(18)19/h2-10,18-19H,1H3
InChI key:InChIKey=UGYPOYBNYVOGBD-UHFFFAOYSA-N
SMILES:C(N(C)C1=CC=CC=C1)(=O)C2=CC=C(B(O)O)C=C2
Synonyms:
  • Boronic acid, [4-[(methylphenylamino)carbonyl]phenyl]-
  • B-[4-[(Methylphenylamino)carbonyl]phenyl]boronic acid
  • Boronic acid, B-[4-[(methylphenylamino)carbonyl]phenyl]-
  • (4-(Methyl(phenyl)carbamoyl)phenyl)boronic acid
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