Acetone oxime (127-06-0)

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  25 g
  $13.00

  100 g
  $39.00

  500 g
  $126.00

Most-cited Publications

• Obtention d'amines primaires par action d'organo-magnesiens sur l'acetoxime (Tetrahedron Letters, 1972)
• The crystal structure of acetoxime (Acta Crystallographica, 1951)
• Reversion of Structure-Activity Relationships of Antitumor Platinum Complexes by Acetoxime but Not Hydroxylamine Ligands (Molecular Pharmacology, 2006)
• Sex and organ differences in oxidative DNA and RNA damage due to treatment of Sprague-Dawley rats with acetoxime or 2-nitropropane (Carcinogenesis, 1990)
• Controlled synthesis of poly(acetone oxime acrylate) as a new reactive polymer: Stimuli-responsive reactive copolymers (European Polymer Journal, 2007)
• Theoretical and experimental study of the orientational nitrogen lone-pair effect on 1J(13C13C) couplings in acetoxime (Journal of Magnetic Resonance, 1989)

Areas of Application

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Trends

Alternate Names

• acetoxime
• acetone, oxime
• actone oxime
• acetoxime, 2-(14)C-labeled
• SMILES
  CC(=NO)C
• InChIKey
  PXAJQJMDEXJWFB-UHFFFAOYSA-N

External Links

• Pubchem - Acetone oxime
• Wikipedia - acetoxime
  Acetone oxime (acetoxime) is the organic compound with the formula (CH3)2CNOH. It is the simplest example of a ketoxime. It is a white crystalline solid that is soluble in water, ethanol, ether, chloroform, and ligroin.

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Acetone oxime

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