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1-Phenyl-1,2-propanedione-2-oxime

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1-Phenyl-1,2-propanedione-2-oxime Basic information

Product Name:
1-Phenyl-1,2-propanedione-2-oxime
Synonyms:
  • A-OXIMINOPROPIOPHENONE
  • ISONITROSO PROPIOPHENONE
  • ALPHA-ISONITROSOPROPIOPHENONE
  • 1-PHENYL-1,2-PROPANEDIONE-2-OXIME
  • 2-ISONITROSOPROPIOPHENONE
  • 2-HYDROXYIMINOPROPIOPHENONE
  • Methylbenzoyl ketone oxime
  • α-(Hydroxyimino)propiophenone
CAS:
119-51-7
MF:
C9H9NO2
MW:
163.17
EINECS:
204-329-2
Product Categories:
  • Functional Materials
  • Photopolymerization Initiators
Mol File:
119-51-7.mol
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1-Phenyl-1,2-propanedione-2-oxime Chemical Properties

Melting point:
113-115 °C(lit.)
Boiling point:
290.25°C (rough estimate)
Density 
1.2021 (rough estimate)
refractive index 
1.5460 (estimate)
storage temp. 
2-8°C
solubility 
soluble in Methanol
form 
Crystals
pka
9.28±0.10(Predicted)
color 
White to light yellow
λmax
398nm(MeOH)(lit.)
CAS DataBase Reference
119-51-7(CAS DataBase Reference)
NIST Chemistry Reference
1-Phenyl-1,2-propane-dione-2-oxime(119-51-7)
EPA Substance Registry System
1,2-Propanedione, 1-phenyl-, 2-oxime (119-51-7)
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Safety Information

Hazard Codes 
Xn
Risk Statements 
20/21/22-36/37/38
Safety Statements 
24/25-37/39-26
WGK Germany 
2
RTECS 
UH2975000
HS Code 
29280090

MSDS

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1-Phenyl-1,2-propanedione-2-oxime Usage And Synthesis

Chemical Properties

WHITE TO LIGHT YELLOW CRYSTALS

Uses

Reactant involved in synthesis of:

  • Cyclometalated iridium complexes for photophysical and electrochemical studies
  • Hydroimidazothiazoles via iodination and cyclization reactions

Reactant involved in:
  • Sonogashira coupling reactions
  • Allylation of aromatic aldehydes using imidazole oside catalysts
  • Beckmann rearrangement of α-oximinoketones

Reagent used in the colorimetric determination of urea

Synthesis Reference(s)

Organic Syntheses, Coll. Vol. 2, p. 363, 1943
Tetrahedron Letters, 30, p. 2833, 1989 DOI: 10.1016/S0040-4039(00)99137-8

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