ChemicalBook--->CAS DataBase List--->359821-38-8

359821-38-8

359821-38-8 Structure

359821-38-8 Structure
IdentificationBack Directory
[Name]

2-amino-N-(2,2,2-trifluoroethyl)acetamide
[CAS]

359821-38-8
[Synonyms]

2-amino-N-(2,2,2-trifluoroethyl)acetamide
Acetamide, 2-?amino-?N-?(2,?2,?2-?trifluoroethyl)?-
[Molecular Formula]

C4H7F3N2O
[MDL Number]

MFCD09944516
[MOL File]

359821-38-8.mol
[Molecular Weight]

156.11
Chemical PropertiesBack Directory
[Boiling point ]

227.5±40.0 °C(Predicted)
[density ]

1.294±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Inert atmosphere,Room temperature
[pka]

12.87±0.46(Predicted)
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P271-P261
Hazard InformationBack Directory
[Uses]

2-amino-N-(2,2,2-trifluoroethyl) acetamide, which is usually stable in the form of salt, is a key intermediate in the synthesis of fluralaner, a new broad-spectrum veterinary insecticide. 
[Preparation]

The method of preparing 2-amino-N-(2,2,2-trifluoroethyl) acetamide and its salt is to react the glycine protected by N-phthalyl group with trifluoroethylamine or its salt to form an amide, and remove the protective group under the action of hydrated fibril to obtain the crude product of 2- amino-N-(2,2,2-trifluoroethyl) acetamide.The crude product can be salted with acid to get a salt of 2-amino-N-(2,2, 2-trifluoroethyl) acetamide, and finally add a base to dissociate pure 2-amino-N-(2,2, 2-trifluoroethyl) ethylkuroamine.
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