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186685-89-2

186685-89-2 Structure

186685-89-2 Structure
IdentificationMore
[Name]

2-(4-FORMYL-2-METHOXY-PHENOXY)-ACETAMIDE
[CAS]

186685-89-2
[Synonyms]

AKOS B000358
AKOS BBS-00006760
CHEMBRDG-BB 4132412
ART-CHEM-BB B000358
TIMTEC-BB SBB009162
2-(4-Formyl-2-methoxyphenoxy)
2-(4-FORMYL-2-METHOXY-PHENOXY)-ACETAMIDE
4-CARBAMOYLMETHOXY-3-METHOXYBENZALDEHYDE
Acetamide, 2-(4-formyl-2-methoxyphenoxy)-
4-(2-Amino-2-oxoethoxy)-3-methoxybenzaldehyde
2-([4-FORMYL-2-(METHYLOXY)PHENYL]OXY)ACETAMIDE
2-(4-formyl-2-methoxyphenoxy)acetamide(SALTDATA: FREE)
[Molecular Formula]

C10H11NO4
[MDL Number]

MFCD01050452
[Molecular Weight]

209.2
[MOL File]

186685-89-2.mol
Chemical PropertiesBack Directory
[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)
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P264-P280-P302+P352-P321-P332+P313-P362-P264-P280-P305+P351+P338-P337+P313P
[Hazard Codes ]

Xi
[Hazard Note ]

Irritant
[HazardClass ]

IRRITANT
[HS Code ]

2912490090
Spectrum DetailBack Directory
[Spectrum Detail]

2-(4-FORMYL-2-METHOXY-PHENOXY)-ACETAMIDE(186685-89-2)1HNMR
Hazard InformationBack Directory
[Synthesis]

Vanillin

121-33-5

Chloroacetamide

79-07-2

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

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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