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Atomfair Benzoic acid, 3-methyl-2-nitro-, methyl ester C9H9NO4
Description Methyl 3-methyl-2-nitrobenzoate (CAS No. 5471-82-9) is a high-purity nitroaromatic ester with the molecular formula C9H9NO4. This compound is a valuable intermediate in organic synthesis, particularly in the preparation of pharmaceuticals, agrochemicals, and specialty chemicals. Its well-defined structure, featuring a methyl ester group adjacent to a nitro substituent on a methylated benzene ring, makes it a versatile building block for nucleophilic substitution and reduction reactions. Available in >98% purity (GC), this product is rigorously tested for consistency and stability, ensuring optimal performance in research and industrial applications. Packaged under inert gas to prevent degradation, it is supplied in amber glass…
Description
Description
Methyl 3-methyl-2-nitrobenzoate (CAS No. 5471-82-9) is a high-purity nitroaromatic ester with the molecular formula C9H9NO4. This compound is a valuable intermediate in organic synthesis, particularly in the preparation of pharmaceuticals, agrochemicals, and specialty chemicals. Its well-defined structure, featuring a methyl ester group adjacent to a nitro substituent on a methylated benzene ring, makes it a versatile building block for nucleophilic substitution and reduction reactions. Available in >98% purity (GC), this product is rigorously tested for consistency and stability, ensuring optimal performance in research and industrial applications. Packaged under inert gas to prevent degradation, it is supplied in amber glass vials or bulk quantities with detailed technical data sheets.
- CAS No: 5471-82-9
- Molecular Formula: C9H9NO4
- Molecular Weight: 195.17
- Exact Mass: 195.05315777
- Monoisotopic Mass: 195.05315777
- IUPAC Name: methyl 3-methyl-2-nitrobenzoate
- SMILES: CC1=C(C(=CC=C1)C(=O)OC)[N+](=O)[O-]
- Synonyms: Methyl 3-methyl-2-nitrobenzoate, 5471-82-9, Benzoic acid, 3-methyl-2-nitro-, methyl ester, 3-Methyl-2-nitrobenzoic Acid Methyl Ester, 67XCE2UHV8
Application
Methyl 3-methyl-2-nitrobenzoate serves as a key precursor in the synthesis of fine chemicals and active pharmaceutical ingredients (APIs), particularly in constructing heterocyclic frameworks. Its nitro group enables facile reduction to amines for further functionalization, while the ester moiety allows hydrolysis or transesterification. Researchers utilize this compound in palladium-catalyzed cross-coupling reactions and as a substrate for studying electrophilic aromatic substitution kinetics. In material science, it contributes to the development of nitroaromatic-based polymers with tailored electronic properties.
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