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Atomfair Tert-butyl 3-nitrobenzoate C11H13NO4

Description Tert-butyl 3-nitrobenzoate (CAS No. 58656-99-8) is a high-purity organic compound with the molecular formula C11H13NO4. This ester derivative of 3-nitrobenzoic acid features a tert-butyl group, enhancing its stability and solubility for synthetic applications. Ideal for researchers in organic chemistry and pharmaceutical development, this compound is rigorously tested to meet analytical standards (typically ??95% purity by HPLC or GC). Supplied as a crystalline solid or powder, it is packaged under inert conditions to ensure long-term stability. Tert-butyl 3-nitrobenzoate is a versatile building block for nucleophilic substitutions, cross-coupling reactions, and the synthesis of complex nitroaromatic intermediates. Store in a cool, dry…

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Description

Description

Tert-butyl 3-nitrobenzoate (CAS No. 58656-99-8) is a high-purity organic compound with the molecular formula C11H13NO4. This ester derivative of 3-nitrobenzoic acid features a tert-butyl group, enhancing its stability and solubility for synthetic applications. Ideal for researchers in organic chemistry and pharmaceutical development, this compound is rigorously tested to meet analytical standards (typically ??95% purity by HPLC or GC). Supplied as a crystalline solid or powder, it is packaged under inert conditions to ensure long-term stability. Tert-butyl 3-nitrobenzoate is a versatile building block for nucleophilic substitutions, cross-coupling reactions, and the synthesis of complex nitroaromatic intermediates. Store in a cool, dry place away from light and oxidizing agents.

  • CAS No: 58656-99-8
  • Molecular Formula: C11H13NO4
  • Molecular Weight: 223.22
  • Exact Mass: 223.08445790
  • Monoisotopic Mass: 223.08445790
  • IUPAC Name: tert-butyl 3-nitrobenzoate
  • SMILES: CC(C)(C)OC(=O)C1=CC(=CC=C1)[N+](=O)[O-]
  • Synonyms: Tert-butyl 3-nitrobenzoate, 58656-99-8, DTXSID10474798, DTXCID40425612, 3-nitro-benzoic acid tert-butyl ester

Application

Tert-butyl 3-nitrobenzoate serves as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and specialty materials. Its nitro group enables facile reduction to amines or participation in metal-catalyzed coupling reactions. Researchers utilize this compound to construct benzoate-based scaffolds in drug discovery. It is also employed in polymer chemistry as a monomer or modifying agent.

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