Description

2,5-Dibromo-4-nitro-1H-imidazole (CAS No. 6154-30-9) is a high-purity halogenated nitroimidazole compound with the molecular formula C₃HBr₂N₃O₂. This versatile heterocyclic organic intermediate is specifically designed for advanced synthetic applications in pharmaceutical research, agrochemical development, and material science. With its dibromo and nitro functional groups, this compound exhibits exceptional reactivity for nucleophilic substitutions, cross-coupling reactions, and as a building block for complex molecular architectures. Our product undergoes rigorous QC testing including HPLC, NMR, and mass spectrometry to ensure ≥98% purity, making it ideal for precision chemistry applications. Supplied as a crystalline solid with comprehensive technical data, SDS, and batch-specific certificates of analysis.

Properties

• CAS Number: 6154-30-9
• Complexity: 149
• IUPAC Name: 2,4-dibromo-5-nitro-1H-imidazole
• InChI: InChI=1S/C3HBr2N3O2/c4-1-2(8(9)10)7-3(5)6-1/h(H,6,7)
• InChI Key: ZGEMTDYSQTXJOF-UHFFFAOYSA-N
• Exact Mass: 270.84150
• Molecular Formula: C3HBr2N3O2
• Molecular Weight: 270.87
• SMILES: C1(=C(N=C(N1)Br)Br)[N+](=O)[O-]
• Topological: 74.5
• Monoisotopic Mass: 268.84355
• Synonyms: 2,5-dibromo-4-nitro-1H-imidazole, 6154-30-9, 2,5-Dibromo-4-nitroimidazole, 2,4-Dibromo-5-nitro-1H-imidazole, 2,4-Dibromo-5-nitroimidazole, 1H-Imidazole, 2,4-dibromo-5-nitro-, Imidazole, 2,4-dibromo-5-nitro-, NSC 222400, MFCD11877989, NSC222400, SCHEMBL58940, Imidazole,4-dibromo-5-nitro-, SCHEMBL3108876, DTXSID80210529, 1H-Imidazole,4-dibromo-5-nitro-, BBL032072, SBB083459, STL373262, AKOS005169805, 2,4-Dibromo-5-nitro-1H-imidazole #, MB10621, NSC-222400, DS-18292, DB-072979, CS-0060033, N10596

This compound serves as a key intermediate in the synthesis of bioactive molecules, particularly in developing antimicrobial and antiparasitic agents. Researchers utilize its reactive bromine sites for palladium-catalyzed coupling reactions to create diverse imidazole derivatives. In material science, it functions as a precursor for functionalized polymers and coordination complexes. The nitro group enables further transformations via reduction to amino derivatives or participation in cyclization reactions.

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