Atomfair 3-(p-Tolylcarbamoyl)phenylboronic acid C14H14BNO3 CAS 1072946-03-2

3-(p-Tolylcarbamoyl)phenylboronic acid (CAS No. 1072946-03-2) is a high-purity boronic acid derivative with the molecular formula C14H14BNO3. This compound, also known by its IUPAC name [3-[(4-methylphenyl)carbamoyl]phenyl]boronic acid , is a valuable building block in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. Its unique structure, featuring a boronic acid group and a p-tolylcarbamoyl moiety, makes it an essential reagent for pharmaceutical research, material science, and chemical biology applications. Our product is rigorously tested for purity (>98%) and stability, ensuring optimal performance in sensitive reactions. Supplied as a white to off-white crystalline powder, it is packaged under inert conditions to maintain integrity.

Description

3-(p-Tolylcarbamoyl)phenylboronic acid (CAS No. 1072946-03-2) is a high-purity boronic acid derivative with the molecular formula C14H14BNO3. This compound, also known by its IUPAC name [3-[(4-methylphenyl)carbamoyl]phenyl]boronic acid, is a valuable building block in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. Its unique structure, featuring a boronic acid group and a p-tolylcarbamoyl moiety, makes it an essential reagent for pharmaceutical research, material science, and chemical biology applications. Our product is rigorously tested for purity (>98%) and stability, ensuring optimal performance in sensitive reactions. Supplied as a white to off-white crystalline powder, it is packaged under inert conditions to maintain integrity.

Properties

  • CAS Number: 1072946-03-2
  • Complexity: 303
  • IUPAC Name: [3-(p-tolylcarbamoyl)phenyl]boronic acid
  • InChI: InChI=1S/C14H14BNO3/c1-10-5-7-13(8-6-10)16-14(17)11-3-2-4-12(9-11)15(18)19/h2-9,18-19H,1H3,(H,16,17)
  • InChI Key: CCZJEJMKNHPTNG-UHFFFAOYSA-N
  • Exact Mass: 255.1066735
  • Molecular Formula: C14H14BNO3
  • Molecular Weight: 255.08
  • SMILES: B(C1=CC(=CC=C1)C(=O)NC2=CC=C(C=C2)C)(O)O
  • Topological: 69.6
  • Monoisotopic Mass: 255.1066735
  • Synonyms: 1072946-03-2, 3-(p-Tolylcarbamoyl)phenylboronic acid, (3-(p-Tolylcarbamoyl)phenyl)boronic acid, [3-[(4-methylphenyl)carbamoyl]phenyl]boronic acid, {3-[(4-Methylphenyl)carbamoyl]phenyl}boronic acid, MFCD10699620, SCHEMBL27194943, DTXSID80674440, AKOS015840461, (3-(p-Tolylcarbamoyl)phenyl)boronicacid, AS-64386, CS-0153055, I12224

Application

3-(p-Tolylcarbamoyl)phenylboronic acid is widely used as a key intermediate in the synthesis of bioactive compounds and pharmaceutical agents. Its boronic acid group enables efficient cross-coupling reactions for constructing complex aromatic systems. Researchers utilize this compound in the development of enzyme inhibitors and receptor modulators due to its ability to form stable interactions with biomolecules. Additionally, it serves as a precursor in materials science for designing functionalized polymers and sensors.

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Disclaimer

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