Basic information Safety Supplier Related

2-(4-FORMYL-2-METHOXY-PHENOXY)-ACETAMIDE

Basic information Safety Supplier Related

2-(4-FORMYL-2-METHOXY-PHENOXY)-ACETAMIDE Basic information

Product Name:
2-(4-FORMYL-2-METHOXY-PHENOXY)-ACETAMIDE
Synonyms:
  • 4-(2-Amino-2-oxoethoxy)-3-methoxybenzaldehyde
  • 2-(4-formyl-2-methoxyphenoxy)acetamide(SALTDATA: FREE)
  • CHEMBRDG-BB 4132412
  • ART-CHEM-BB B000358
  • 2-([4-FORMYL-2-(METHYLOXY)PHENYL]OXY)ACETAMIDE
  • 2-(4-FORMYL-2-METHOXY-PHENOXY)-ACETAMIDE
  • AKOS BBS-00006760
  • AKOS B000358
CAS:
186685-89-2
MF:
C10H11NO4
MW:
209.2
Mol File:
186685-89-2.mol
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2-(4-FORMYL-2-METHOXY-PHENOXY)-ACETAMIDE Chemical Properties

Melting point:
84-85 °C(Solv: benzene (71-43-2))
Boiling point:
452.0±35.0 °C(Predicted)
Density 
1.257±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
pka
15.30±0.40(Predicted)
Appearance
Off-white to light yellow Solid
CAS DataBase Reference
186685-89-2(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
HazardClass 
IRRITANT
HS Code 
2912490090
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2-(4-FORMYL-2-METHOXY-PHENOXY)-ACETAMIDE Usage And Synthesis

Synthesis

121-33-5

79-07-2

186685-89-2

General procedure for the synthesis of 2-(4-formyl-2-methoxyphenyl)acetamide from vanillin and chloroacetamide: In a solvent mixture of acetonitrile-DMF (20 mL, 8:2, v/v), chloroacetamide (0.010 mol), vanillin (0.011 mol), and potassium carbonate (2.00 g, 0.0145 mol) were sequentially added. The reaction mixture was heated and refluxed under stirring for 5-7 h. The progress of the reaction was monitored by thin layer chromatography (TLC). Upon completion of the reaction, the solvent was removed by evaporation, the residue was treated with an appropriate amount of water and the precipitated solid was collected by filtration. The resulting precipitate was washed with 30% aqueous methanol and subsequently dried in air. The yield of the product 2-(4-formyl-2-methoxyphenyl)acetamide and its physicochemical properties are listed in Table 9.

References

[1] Russian Chemical Bulletin, 2015, vol. 64, # 2, p. 395 - 404
[2] Izv. Akad. Nauk, Ser. Khim., 2015, # 2, p. 395 - 404,10
[3] Russian Journal of General Chemistry, 2005, vol. 75, # 7, p. 1113 - 1124
[4] European Journal of Medicinal Chemistry, 2014, vol. 81, p. 1 - 14

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