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Atomfair 4-Amino-3-bromo-5-nitrobenzonitrile C7H4BrN3O2
Description 4-Amino-3-bromo-5-nitrobenzonitrile (CAS No. 1239720-33-2) is a high-purity, synthetic organic compound with the molecular formula C7H4BrN3O2. This aromatic nitrile derivative features a strategically functionalized benzene ring with amino, bromo, and nitro substituents, making it a versatile intermediate for pharmaceutical, agrochemical, and materials science research. The compound is supplied as a crystalline solid with ??95% purity (HPLC) and is rigorously tested for consistency, stability, and trace impurities. Ideal for use in cross-coupling reactions, heterocyclic synthesis, and as a building block for advanced molecular architectures. Packaged under inert gas in amber glass vials to ensure long-term stability and shipped with comprehensive analytical…
Description
Description
4-Amino-3-bromo-5-nitrobenzonitrile (CAS No. 1239720-33-2) is a high-purity, synthetic organic compound with the molecular formula C7H4BrN3O2. This aromatic nitrile derivative features a strategically functionalized benzene ring with amino, bromo, and nitro substituents, making it a versatile intermediate for pharmaceutical, agrochemical, and materials science research. The compound is supplied as a crystalline solid with ??95% purity (HPLC) and is rigorously tested for consistency, stability, and trace impurities. Ideal for use in cross-coupling reactions, heterocyclic synthesis, and as a building block for advanced molecular architectures. Packaged under inert gas in amber glass vials to ensure long-term stability and shipped with comprehensive analytical data (MS, 1H/13C NMR, FTIR).
- CAS No: 1239720-33-2
- Molecular Formula: C7H4BrN3O2
- Molecular Weight: 242.03
- Exact Mass: 240.94869
- Monoisotopic Mass: 240.94869
- IUPAC Name: 4-amino-3-bromo-5-nitrobenzonitrile
- SMILES: C1=C(C=C(C(=C1[N+](=O)[O-])N)Br)C#N
- Synonyms: 4-Amino-3-bromo-5-nitrobenzonitrile, 1239720-33-2, DTXSID50604895, DTXCID10555652, 816-710-6
Application
4-Amino-3-bromo-5-nitrobenzonitrile serves as a key precursor in the synthesis of bioactive heterocycles, particularly in the development of kinase inhibitors and antimicrobial agents. Its electron-deficient aromatic system enables efficient participation in Buchwald-Hartwig aminations and Suzuki-Miyaura cross-coupling reactions. Researchers utilize this compound to construct complex polycyclic frameworks for drug discovery programs targeting inflammatory and oncological pathways.
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