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Atomfair 4-Bromo-3-phenyl-1H-pyrazole C9H7BrN2

Description 4-Bromo-3-phenyl-1H-pyrazole (CAS No. 13808-65-6) is a high-purity heterocyclic organic compound with the molecular formula C9H7BrN2. This brominated pyrazole derivative features a phenyl substituent at the 3-position, making it a versatile intermediate for pharmaceutical, agrochemical, and materials science research. Its well-defined structure (IUPAC name: 4-bromo-5-phenyl-1H-pyrazole) ensures consistent reactivity in cross-coupling reactions, metal-catalyzed transformations, and as a building block for bioactive molecules. Available in >98% purity (HPLC), this compound is supplied in sealed packaging under inert conditions to ensure stability. Ideal for medicinal chemistry, ligand synthesis, and structural studies.

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Description

Description

4-Bromo-3-phenyl-1H-pyrazole (CAS No. 13808-65-6) is a high-purity heterocyclic organic compound with the molecular formula C9H7BrN2. This brominated pyrazole derivative features a phenyl substituent at the 3-position, making it a versatile intermediate for pharmaceutical, agrochemical, and materials science research. Its well-defined structure (IUPAC name: 4-bromo-5-phenyl-1H-pyrazole) ensures consistent reactivity in cross-coupling reactions, metal-catalyzed transformations, and as a building block for bioactive molecules. Available in >98% purity (HPLC), this compound is supplied in sealed packaging under inert conditions to ensure stability. Ideal for medicinal chemistry, ligand synthesis, and structural studies.

  • CAS No: 13808-65-6
  • Molecular Formula: C9H7BrN2
  • Molecular Weight: 223.07
  • Exact Mass: 221.97926
  • Monoisotopic Mass: 221.97926
  • IUPAC Name: 4-bromo-5-phenyl-1H-pyrazole
  • SMILES: C1=CC=C(C=C1)C2=C(C=NN2)Br
  • Synonyms: 4-Bromo-3-phenyl-1H-pyrazole, 13808-65-6, 4-bromo-3-phenylpyrazole, DTXSID40415917, DTXCID70366766

Application

4-Bromo-3-phenyl-1H-pyrazole serves as a key precursor in Suzuki-Miyaura and Buchwald-Hartwig coupling reactions for drug discovery. Researchers utilize it to develop kinase inhibitors and antimicrobial agents due to its privileged pyrazole scaffold. The compound is also employed in coordination chemistry to synthesize transition metal complexes for catalytic applications.

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