Description
N-(4-bromophenyl)-2-nitroaniline (CAS No. 58476-59-8) is a high-purity organic compound with the molecular formula C12H9BrN2O2. This yellow to orange crystalline powder is widely utilized in chemical research and pharmaceutical synthesis due to its unique structural properties. With a molecular weight of 293.12 g/mol, it serves as a versatile intermediate in the preparation of dyes, agrochemicals, and advanced materials. Our product is rigorously tested to ensure ≥98% purity (HPLC) and is supplied in sealed packaging to maintain stability. Ideal for Suzuki coupling reactions and other cross-coupling methodologies, this compound is a valuable asset for researchers exploring nitroaromatic and brominated aromatic systems.
Properties
- CAS Number: 58476-59-8
- Complexity: 262
- IUPAC Name: N-(4-bromophenyl)-2-nitro-aniline
- InChI: InChI=1S/C12H9BrN2O2/c13-9-5-7-10(8-6-9)14-11-3-1-2-4-12(11)15(16)17/h1-8,14H
- InChI Key: GMFUKKONFZISMI-UHFFFAOYSA-N
- Exact Mass: 291.98474
- Molecular Formula: C12H9BrN2O2
- Molecular Weight: 293.12
- SMILES: C1=CC=C(C(=C1)NC2=CC=C(C=C2)Br)[N+](=O)[O-]
- Topological: 57.9
- Monoisotopic Mass: 291.98474
- Synonyms: N-(4-bromophenyl)-2-nitroaniline, 58476-59-8, N-(4-BROMOPHENYL)-2-NITROBENZENAMINE, MFCD00092900, (4-bromophenyl)-(2-nitrophenyl) amine, N-(4-BROMOPHENYL)-2-NITROBENZAMINE, 4-bromo-N-(2-nitrophenyl)benzenamine, SCHEMBL338789, DTXSID20475559, GMFUKKONFZISMI-UHFFFAOYSA-N, STL480853, (4-bromophenyl)-(2-nitrophenyl)amine, AKOS027254686, (4-bromophenyl)-(2-nitrophenyl)-amine, (4-Bromo-phenyl)-(2-nitro-phenyl)amine, AS-30097, SY094353, (4-bromo-phenyl)-(2-nitro-phenyl)-amine, DB-340187, CS-0060479
Application
N-(4-bromophenyl)-2-nitroaniline is primarily employed as a key intermediate in organic synthesis, particularly in the development of pharmaceutical compounds and specialty chemicals. Its bromophenyl and nitroaniline moieties make it suitable for palladium-catalyzed cross-coupling reactions. Researchers also utilize this compound in the synthesis of liquid crystals and optoelectronic materials. The nitro group offers potential for further functionalization through reduction to amines or conversion to other derivatives.
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