Description

1-(4-Bromophenyl)-2-phenyl-1H-benzo[d]imidazole (CAS No. 760212-58-6) is a high-purity benzimidazole derivative with the molecular formula C₁₉H₁₃BrN₂. This compound features a bromophenyl group at the 1-position and a phenyl group at the 2-position of the benzimidazole core, making it a valuable intermediate for organic synthesis and pharmaceutical research. Its well-defined structure and high chemical stability ensure reliable performance in coupling reactions, heterocyclic chemistry, and as a building block for advanced materials. Suitable for researchers and scientists, this product is rigorously tested for purity and consistency, ensuring optimal results in your experiments. Available in various quantities to meet both small-scale and bulk requirements.

Properties

• CAS Number: 760212-58-6
• Complexity: 360
• IUPAC Name: 1-(4-bromophenyl)-2-phenyl-benzimidazole
• InChI: InChI=1S/C19H13BrN2/c20-15-10-12-16(13-11-15)22-18-9-5-4-8-17(18)21-19(22)14-6-2-1-3-7-14/h1-13H
• InChI Key: PPYIZNYOMNYZCG-UHFFFAOYSA-N
• Exact Mass: 348.02621
• Molecular Formula: C19H13BrN2
• Molecular Weight: 349.2
• SMILES: C1=CC=C(C=C1)C2=NC3=CC=CC=C3N2C4=CC=C(C=C4)Br
• Topological: 17.8
• Monoisotopic Mass: 348.02621
• Synonyms: 760212-58-6, 1-(4-bromophenyl)-2-phenyl-1H-benzo[d]imidazole, 1-(4-Bromophenyl)-2-phenylbenzimidazole, 1H-BenziMidazole, 1-(4-broMophenyl)-2-phenyl, 1-(4-bromophenyl)-2-phenyl-1H-benzimidazole, MFCD09746342, 1-(4-bromophenyl)-2-phenyl-1H-1,3-benzodiazole, 1-(4-Bromophenyl)-2-phenyl-1H-benzo[d]imidazole;1H-Benzimidazole, 1-(4-bromophenyl)-2-phenyl-, SCHEMBL339108, DTXSID60630569, PPYIZNYOMNYZCG-UHFFFAOYSA-N, AKOS015994855, AS-67295, DA-31054, SY022108, B4929, CS-0156363, F16010, 1-(4-Bromophenyl)-2-phenyl-1H-benzo[d]imidazole;1H-enzimidazole, 1-(4-romophenyl)-2-henyl-

Application

1-(4-Bromophenyl)-2-phenyl-1H-benzo[d]imidazole is widely used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and anticancer agents. Its benzimidazole core makes it a versatile scaffold for designing novel heterocyclic compounds with potential biological activity. Researchers also utilize this compound in material science for the preparation of organic semiconductors and luminescent materials. Its bromine substituent allows for further functionalization via cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions.

If you are interested or have any questions, please contact us at support@atomfair.com

Disclaimer: Sold exclusively for laboratory research. Prohibited for commercial use, diagnostics, or human/animal applications. Buyers assume all compliance liability.