ChemicalBook > CAS DataBase List > 2-(hydroxyimino)-2-phenylacetaldehyde oxime

2-(hydroxyimino)-2-phenylacetaldehyde oxime

Product Name
2-(hydroxyimino)-2-phenylacetaldehyde oxime
CAS No.
4589-97-3
Chemical Name
2-(hydroxyimino)-2-phenylacetaldehyde oxime
Synonyms
phenylglyoxime;1-Phenylglyoxal dioxime;α-(Hydroxyimino)benzeneacetaldehyde oxime;2-(hydroxyimino)-2-phenylacetaldehyde oxime;Benzeneacetaldehyde, α-(hydroxyimino)-, oxime
CBNumber
CB9908161
Molecular Formula
C8H8N2O2
Formula Weight
164.16132
MOL File
4589-97-3.mol
More
Less

2-(hydroxyimino)-2-phenylacetaldehyde oxime Property

Melting point:
180 °C
Boiling point:
291.62°C (rough estimate)
Density 
1.2739 (rough estimate)
refractive index 
1.6000 (estimate)
pka
9.52±0.10(Predicted)
More
Less

Hazard and Precautionary Statements (GHS)

More
Less

N-Bromosuccinimide Price

American Custom Chemicals Corporation
Product number
CHM0304674
Product name
2-(HYDROXYIMINO)-2-PHENYLACETALDEHYDE OXIME
Purity
95.00%
Packaging
5MG
Price
$500.4
Updated
2021/12/16
More
Less

2-(hydroxyimino)-2-phenylacetaldehyde oxime Chemical Properties,Usage,Production

Preparation

To a solution of 50 gm (0.34 mole) of ω-oximinoacetophenone (ω-isonitrosoacetophenone) in 150 ml of ethanol is added to a solution of 48 gm (0.595 mole) of sodium acetate and 24 gm (0.345 mole) of hydrox­ylamine hydrochloride in 75 ml of water. The mixture is heated at reflux for 4 hr. After cooling, a large portion of the Solvent is evaporated off under reduced pressure. The mixed crude product, which precipitates, is filtered off, washed with water, and air-dried to afford 51 gm (92%), m.p. 150-158°C.
The separation of the three isomers by fractional crystallization pro­cedures depends on the relative ratio of the components in the mixture, the concentration of the components in the solvent, the length of time the solvent-product mixture is heated, etc. It is therefore important that the progress of the crystallization be followed by thin-layer chromatography using freshly prepared tic plates [Merck (Darmstadt) silica gel G is recom­mended as the coating]. The suggested tic solvent is benzene-ethyl acetate (7:3), detection by iodine vapor; 0.45 Rf for phenyl-amphi-glyoxime (I), 0.40 Rf for phenyl-anti-glyoxime (II), and 0.35 Rf for phenyl-syn-glyoxime(III).

Anti-glyoxime (II), and 0.35 Rf for phenyl-syn-glyoxime(III). Anti-phenyl-amphi-glyoxime (I) is separated from the mixed product by repeated recrystallization from acetone-chloroform (or alcohol-water), m.p. 178-180°C; UV, λmax (95% ethanol) 230 mμ (ε 14,800).
Phenyl-anti-glyoxime (II) is isolated from the mother liquor of the first crystallization in the separation of (I). The residue from the evaporation of this mother liquor is crystallized repeatedly from acetone-chloroform. After sublimation, the properties of the material are as follows: sublima­tion temperature, 90°C (0.2 mm Hg); m.p. 166-168°C; UV, λmax (95% ethanol) 228 mμ (ε 14,380). Only about 1% of pure isomer is isolated from the starting product.
Phenyl-syn-glyoxime (III) is isolated by crystallizing the starting product from a dilute solution of ethyl acetate, m.p. 168-170°C; UV, λmax (95% ethanol) 252 mμ (ε 12,200).

2-(hydroxyimino)-2-phenylacetaldehyde oxime Preparation Products And Raw materials

Raw materials

Preparation Products

More
Less

2-(hydroxyimino)-2-phenylacetaldehyde oxime Suppliers

4589-97-3, 2-(hydroxyimino)-2-phenylacetaldehyde oximeRelated Search:


  • phenylglyoxime
  • 2-(hydroxyimino)-2-phenylacetaldehyde oxime
  • 1-Phenylglyoxal dioxime
  • α-(Hydroxyimino)benzeneacetaldehyde oxime
  • Benzeneacetaldehyde, α-(hydroxyimino)-, oxime
  • 4589-97-3