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Atomfair Diethyl 5-methylpyridine-2,3-dicarboxylate C12H15NO4

Description Diethyl 5-methylpyridine-2,3-dicarboxylate (CAS No. 105151-48-2) is a high-purity organic compound with the molecular formula C12H15NO4. This ester derivative of pyridine-2,3-dicarboxylic acid features two ethyl ester groups and a methyl substituent at the 5-position, making it a versatile intermediate for pharmaceutical, agrochemical, and materials science research. Its well-defined structure and reactivity enable applications in heterocyclic synthesis, ligand design, and coordination chemistry. Available in >98% purity (HPLC), this compound is supplied in rigorously tested batches to ensure consistency for demanding laboratory applications. Store under inert atmosphere at 2-8??C to maintain stability.

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Description

Description

Diethyl 5-methylpyridine-2,3-dicarboxylate (CAS No. 105151-48-2) is a high-purity organic compound with the molecular formula C12H15NO4. This ester derivative of pyridine-2,3-dicarboxylic acid features two ethyl ester groups and a methyl substituent at the 5-position, making it a versatile intermediate for pharmaceutical, agrochemical, and materials science research. Its well-defined structure and reactivity enable applications in heterocyclic synthesis, ligand design, and coordination chemistry. Available in >98% purity (HPLC), this compound is supplied in rigorously tested batches to ensure consistency for demanding laboratory applications. Store under inert atmosphere at 2-8??C to maintain stability.

  • CAS No: 105151-48-2
  • Molecular Formula: C12H15NO4
  • Molecular Weight: 237.25
  • Exact Mass: 237.10010796
  • Monoisotopic Mass: 237.10010796
  • IUPAC Name: diethyl 5-methylpyridine-2,3-dicarboxylate
  • SMILES: CCOC(=O)C1=C(N=CC(=C1)C)C(=O)OCC
  • Synonyms: 105151-48-2, Diethyl 5-methylpyridine-2,3-dicarboxylate, Diethyl 5-methyl-2,3-pyridinedicarboxylate, 2,3-DIETHYL 5-METHYLPYRIDINE-2,3-DICARBOXYLATE, 2,3-Pyridinedicarboxylic acid, 5-methyl-, diethyl ester

Application

Diethyl 5-methylpyridine-2,3-dicarboxylate serves as a key building block for synthesizing complex nitrogen-containing heterocycles in medicinal chemistry. Researchers utilize it to develop novel pharmaceutical candidates targeting CNS disorders and anti-inflammatory pathways. The compound’s ester groups facilitate further functionalization through hydrolysis or transesterification reactions, while the methyl substitution allows regioselective modifications.

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