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Atomfair (E)-Methyl 2-(((2,2-dimethoxyethyl)amino)methylene)-4-methoxy-3-oxobutanoate C11H19NO6

Description (E)-Methyl 2-(((2,2-dimethoxyethyl)amino)methylene)-4-methoxy-3-oxobutanoate (CAS: 1646862-12-5) is a high-purity, synthetic organic compound with the molecular formula C11H19NO6. This specialized chemical features a unique (E)-iminomethyl backbone coupled with dimethoxyethyl and methoxy ester functional groups, making it a versatile intermediate for advanced organic synthesis. With an IUPAC name of methyl (E)-2-(2,2-dimethoxyethyliminomethyl)-3-hydroxy-4-methoxybut-2-enoate , it is supplied as a stable solid with ??95% purity (HPLC), rigorously tested via NMR and LC-MS to ensure batch consistency. Ideal for pharmaceutical research, asymmetric catalysis, and heterocycle construction, this compound is packaged under inert gas in amber glass vials to prevent degradation. Store at 2-8??C in a dry environment.

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Description

Description

(E)-Methyl 2-(((2,2-dimethoxyethyl)amino)methylene)-4-methoxy-3-oxobutanoate (CAS: 1646862-12-5) is a high-purity, synthetic organic compound with the molecular formula C11H19NO6. This specialized chemical features a unique (E)-iminomethyl backbone coupled with dimethoxyethyl and methoxy ester functional groups, making it a versatile intermediate for advanced organic synthesis. With an IUPAC name of methyl (E)-2-(2,2-dimethoxyethyliminomethyl)-3-hydroxy-4-methoxybut-2-enoate, it is supplied as a stable solid with ??95% purity (HPLC), rigorously tested via NMR and LC-MS to ensure batch consistency. Ideal for pharmaceutical research, asymmetric catalysis, and heterocycle construction, this compound is packaged under inert gas in amber glass vials to prevent degradation. Store at 2-8??C in a dry environment.

  • CAS No: 1646862-12-5
  • Molecular Formula: C11H19NO6
  • Molecular Weight: 261.27
  • Exact Mass: 261.12123733
  • Monoisotopic Mass: 261.12123733
  • IUPAC Name: methyl (E)-2-(2,2-dimethoxyethyliminomethyl)-3-hydroxy-4-methoxybut-2-enoate
  • SMILES: COC/C(=C(/C=NCC(OC)OC)C(=O)OC)/O
  • Synonyms: methyl 2-(2,2-dimethoxyethyliminomethyl)-3-hydroxy-4-methoxybut-2-enoate, (E)-Methyl 2-(((2,2-dimethoxyethyl)amino)methylene)-4-methoxy-3-oxobutanoate, 1335210-26-8, 1646862-12-5, SCHEMBL2410499

Application

This compound serves as a key building block in the synthesis of complex heterocyclic scaffolds, particularly for drug discovery targeting enzyme inhibition. Its reactive iminomethyl group enables participation in multicomponent reactions (e.g., Ugi-type condensations), while the ??-keto ester moiety facilitates cyclization reactions. Researchers utilize it in developing antimicrobial agents and as a precursor for chiral auxiliaries in asymmetric synthesis.

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