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Atomfair Ethyl 3,5-dinitrobenzoate C9H8N2O6
Description Ethyl 3,5-dinitrobenzoate (CAS No. 618-71-3) is a high-purity nitroaromatic ester with the molecular formula C9H8N2O6. This compound is widely utilized in organic synthesis, pharmaceutical research, and as a derivatization reagent for analytical chemistry applications. Its crystalline structure and well-defined reactivity make it a valuable intermediate for the preparation of more complex nitroaromatic compounds. Ethyl 3,5-dinitrobenzoate is characterized by its high thermal stability and compatibility with a range of solvents, including ethanol, acetone, and dimethyl sulfoxide (DMSO). Suitable for laboratory and industrial-scale use, this product is rigorously tested to ensure ??98% purity (HPLC) and is supplied in sealed containers to…
Description
Description
Ethyl 3,5-dinitrobenzoate (CAS No. 618-71-3) is a high-purity nitroaromatic ester with the molecular formula C9H8N2O6. This compound is widely utilized in organic synthesis, pharmaceutical research, and as a derivatization reagent for analytical chemistry applications. Its crystalline structure and well-defined reactivity make it a valuable intermediate for the preparation of more complex nitroaromatic compounds. Ethyl 3,5-dinitrobenzoate is characterized by its high thermal stability and compatibility with a range of solvents, including ethanol, acetone, and dimethyl sulfoxide (DMSO). Suitable for laboratory and industrial-scale use, this product is rigorously tested to ensure ??98% purity (HPLC) and is supplied in sealed containers to maintain integrity.
- CAS No: 618-71-3
- Molecular Formula: C9H8N2O6
- Molecular Weight: 240.17
- Exact Mass: 240.03823598
- Monoisotopic Mass: 240.03823598
- IUPAC Name: ethyl 3,5-dinitrobenzoate
- SMILES: CCOC(=O)C1=CC(=CC(=C1)[N+](=O)[O-])[N+](=O)[O-]
- Synonyms: Ethyl 3,5-dinitrobenzoate, Benzoic acid, 3,5-dinitro-, ethyl ester, EINECS 210-559-4, DTXSID20210801, NSC 32741
Application
Ethyl 3,5-dinitrobenzoate is commonly employed as a derivatizing agent in gas chromatography (GC) and high-performance liquid chromatography (HPLC) for the identification of alcohols and amines. It serves as a key intermediate in the synthesis of dyes, explosives, and pharmaceutical compounds due to its nitro-functionalized aromatic structure. Researchers also utilize it in kinetic studies and as a standard in spectroscopic analysis.
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