Basic information Safety Supplier Related

4-FLUOROPHENYLGLYOXAL HYDRATE

Basic information Safety Supplier Related

4-FLUOROPHENYLGLYOXAL HYDRATE Basic information

Product Name:
4-FLUOROPHENYLGLYOXAL HYDRATE
Synonyms:
  • 4-FLUOROPHENYLGLYOXAL HYDRATE
  • 4-FLUOROPHENYLGLYOXAL MONOHYDRATE
  • 2-(4-Fluorophenyl)-2-oxo-acetaldehyde
  • 2-(4-fluorophenyl)-2-oxoacetaldehyde hydrate
  • 4-FLUOROPHENYLGLYOXAL HYDRATE , DRY WT. BASIS
  • 4-FLUOROPHENYLGLYOXAL HYDRATE, 98%, DRY WT. BASIS
  • 2-(4-fluorophenyl)-2-keto-acetaldehyde
  • 2-(4-fluorophenyl)-2-oxo-ethanal
CAS:
447-43-8
MF:
C8H7FO3
MW:
170.14
EINECS:
639-289-9
Mol File:
447-43-8.mol
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4-FLUOROPHENYLGLYOXAL HYDRATE Chemical Properties

Melting point:
80 °C
Boiling point:
115 °C
Density 
1.411±0.06 g/cm3(Predicted)
storage temp. 
Inert atmosphere,Store in freezer, under -20°C
form 
solid
pka
10.51±0.41(Predicted)
color 
White
BRN 
2354778
CAS DataBase Reference
447-43-8(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
RTECS 
CY1440000
HazardClass 
IRRITANT
HS Code 
2914790090

MSDS

  • Language:English Provider:ALFA
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4-FLUOROPHENYLGLYOXAL HYDRATE Usage And Synthesis

Synthesis

403-42-9

447-43-8

General procedure for the synthesis of hydrated 4-fluorobenzoylformaldehyde from 4-fluoroacetophenone: general method: a mixture of substrate (0.6 mmol) and bromoethylene (2a, 0.06 mmol) in DMSO (1.1 mL) was placed in an open-topped flask and heated in an oil bath (see Table 2 for specific temperatures and reaction times). After completion of the reaction (monitored by TLC), the reaction mixture was diluted with water (11 mL), treated with saturated NaCl solution and extracted with ethyl acetate (5 × 4 mL). Only in case of synthesis of arylglyoxal, the organic layer was additionally washed with Na2CO3 solution (0.12 mmol, dissolved in 2 mL of water), followed by saturated aqueous NaCl solution and dried with anhydrous Na2SO4. The extract was purified by column chromatography (eluent: petroleum ether/ethyl acetate gradient) to give pure product.

References

[1] Chinese Chemical Letters, 2013, vol. 24, # 12, p. 1118 - 1122
[2] Tetrahedron, 2011, vol. 67, # 41, p. 8000 - 8008
[3] Chemistry of Heterocyclic Compounds, 2018, vol. 54, # 1, p. 51 - 57
[4] Khim. Geterotsikl. Soedin., 2018, vol. 54, # 1, p. 51 - 57,7
[5] Journal of Organic Chemistry, 1952, vol. 17, p. 1425,1429

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