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Atomfair N-(2-hydroxyethyl)acetoacetamide C6H11NO3

Description N-(2-hydroxyethyl)acetoacetamide (CAS No. 24922-02-9) is a high-purity organic compound with the molecular formula C6H11NO3. This versatile chemical, also known by its IUPAC name N-(2-hydroxyethyl)-3-oxobutanamide , features both hydroxyl and amide functional groups, making it valuable for synthetic and biochemical applications. It is supplied as a stable, crystalline solid with a purity of ??98%, ideal for research, pharmaceutical intermediates, and specialty chemical synthesis. Suitable for controlled reactions, it is packaged under inert conditions to ensure longevity and performance. Store in a cool, dry place away from strong oxidizers.

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Description

Description

N-(2-hydroxyethyl)acetoacetamide (CAS No. 24922-02-9) is a high-purity organic compound with the molecular formula C6H11NO3. This versatile chemical, also known by its IUPAC name N-(2-hydroxyethyl)-3-oxobutanamide, features both hydroxyl and amide functional groups, making it valuable for synthetic and biochemical applications. It is supplied as a stable, crystalline solid with a purity of ??98%, ideal for research, pharmaceutical intermediates, and specialty chemical synthesis. Suitable for controlled reactions, it is packaged under inert conditions to ensure longevity and performance. Store in a cool, dry place away from strong oxidizers.

  • CAS No: 24922-02-9
  • Molecular Formula: C6H11NO3
  • Molecular Weight: 145.16
  • Exact Mass: 145.07389321
  • Monoisotopic Mass: 145.07389321
  • IUPAC Name: N-(2-hydroxyethyl)-3-oxobutanamide
  • SMILES: CC(=O)CC(=O)NCCO
  • Synonyms: N-(2-Hydroxyethyl)-3-oxobutanamide, N-(2-Hydroxyethyl)acetoacetamide, Butanamide, N-(2-hydroxyethyl)-3-oxo-, EINECS 246-149-7, 246-149-7

Application

N-(2-hydroxyethyl)acetoacetamide is widely used as a key intermediate in organic synthesis, particularly for pharmaceuticals and agrochemicals. Its reactive keto and hydroxyl groups enable its use in heterocyclic compound formation and polymer modification. Researchers also employ it in peptide coupling and crosslinking applications due to its bifunctional nature.

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