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Atomfair Ethyl 6-formyl-5-nitronicotinate C9H8N2O5

Description Ethyl 6-formyl-5-nitronicotinate (CAS: 2589531-65-5) is a high-purity nitropyridine derivative with the molecular formula C9H8N2O5, widely utilized in pharmaceutical and agrochemical research. This compound, also known by its IUPAC name ethyl 6-formyl-5-nitropyridine-3-carboxylate , features a reactive formyl group and nitro functionality, making it a versatile intermediate for heterocyclic synthesis. With a molecular weight of 224.17 g/mol, it is supplied as a crystalline solid with ??95% purity (HPLC), ensuring optimal performance in coupling reactions, nucleophilic substitutions, and catalyst studies. Ideal for medicinal chemistry, its structural motifs are key to developing kinase inhibitors and antimicrobial agents. Store under inert conditions at 2-8??C…

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Description

Description

Ethyl 6-formyl-5-nitronicotinate (CAS: 2589531-65-5) is a high-purity nitropyridine derivative with the molecular formula C9H8N2O5, widely utilized in pharmaceutical and agrochemical research. This compound, also known by its IUPAC name ethyl 6-formyl-5-nitropyridine-3-carboxylate, features a reactive formyl group and nitro functionality, making it a versatile intermediate for heterocyclic synthesis. With a molecular weight of 224.17 g/mol, it is supplied as a crystalline solid with ??95% purity (HPLC), ensuring optimal performance in coupling reactions, nucleophilic substitutions, and catalyst studies. Ideal for medicinal chemistry, its structural motifs are key to developing kinase inhibitors and antimicrobial agents. Store under inert conditions at 2-8??C to maintain stability.

  • CAS No: 2589531-65-5
  • Molecular Formula: C9H8N2O5
  • Molecular Weight: 224.17
  • Exact Mass: 224.04332136
  • Monoisotopic Mass: 224.04332136
  • IUPAC Name: ethyl 6-formyl-5-nitropyridine-3-carboxylate
  • SMILES: CCOC(=O)C1=CC(=C(N=C1)C=O)[N+](=O)[O-]
  • Synonyms: ethyl 6-formyl-5-nitronicotinate, 2589531-65-5, SCHEMBL25117833, CS-0214373, G15693

Application

Ethyl 6-formyl-5-nitronicotinate serves as a critical building block in the synthesis of bioactive pyridine scaffolds, particularly in drug discovery for targeting enzyme inhibition. Its nitro and formyl groups enable facile functionalization via reduction or condensation reactions, aiding the development of novel anticancer and anti-inflammatory compounds. Researchers also employ it in material science for designing photoactive coordination polymers.

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