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Atomfair 2,4-Dichloro-3,5-dinitrobenzonitrile C7HCl2N3O4
Description 2,4-Dichloro-3,5-dinitrobenzonitrile (CAS No. 19755-53-4) is a high-purity nitroaromatic compound with the molecular formula C7HCl2N3O4. This crystalline solid is characterized by its dichloro and dinitro functional groups attached to a benzonitrile backbone, making it a versatile intermediate in organic synthesis and agrochemical research. With a molecular weight of 261.01 g/mol, it is optimized for precision applications requiring controlled reactivity. Our product is rigorously tested for purity (>98% by HPLC) and stability, ensuring consistent performance in demanding laboratory and industrial processes. Suitable for use as a precursor in heterocyclic chemistry, electrophilic substitution reactions, and specialty chemical manufacturing.
Description
Description
2,4-Dichloro-3,5-dinitrobenzonitrile (CAS No. 19755-53-4) is a high-purity nitroaromatic compound with the molecular formula C7HCl2N3O4. This crystalline solid is characterized by its dichloro and dinitro functional groups attached to a benzonitrile backbone, making it a versatile intermediate in organic synthesis and agrochemical research. With a molecular weight of 261.01 g/mol, it is optimized for precision applications requiring controlled reactivity. Our product is rigorously tested for purity (>98% by HPLC) and stability, ensuring consistent performance in demanding laboratory and industrial processes. Suitable for use as a precursor in heterocyclic chemistry, electrophilic substitution reactions, and specialty chemical manufacturing.
- CAS No: 19755-53-4
- Molecular Formula: C7HCl2N3O4
- Molecular Weight: 262.00
- Exact Mass: 260.9344109
- Monoisotopic Mass: 260.9344109
- IUPAC Name: 2,4-dichloro-3,5-dinitrobenzonitrile
- SMILES: C1=C(C(=C(C(=C1[N+](=O)[O-])Cl)[N+](=O)[O-])Cl)C#N
- Synonyms: 2,4-Dichloro-3,5-dinitrobenzonitrile, 654-706-4, 1930-71-8, 2 4-DICHLORO-3 5-DINITROBENZONITRILE, Benzonitrile, 2,4-dichloro-3,5-dinitro-
Application
2,4-Dichloro-3,5-dinitrobenzonitrile serves as a key intermediate in the synthesis of herbicides and fungicides due to its reactive nitro and chloro groups. Researchers utilize it in electrophilic aromatic substitution studies to explore regioselectivity in poly-substituted benzene derivatives. It is also employed in the development of dyestuffs and as a building block for nitrogen-containing heterocycles in pharmaceutical research.
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