97589-53-2

Basic information

• Product Name: (S)-2,2,2-triuoro-N-(3-methyl-1-oxo-1-phenylbutan-2-yl)acetamide
• Synonyms: (S)-2,2,2-triuoro-N-(3-methyl-1-oxo-1-phenylbutan-2-yl)acetamide
• CAS NO: 97589-53-2
• Molecular Weight: 273.255
• Mol File: 97589-53-2.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (S)-2,2,2-triuoro-N-(3-methyl-1-oxo-1-phenylbutan-2-yl)acetamide(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-2,2,2-triuoro-N-(3-methyl-1-oxo-1-phenylbutan-2-yl)acetamide(97589-53-2)
• EPA Substance Registry System: (S)-2,2,2-triuoro-N-(3-methyl-1-oxo-1-phenylbutan-2-yl)acetamide(97589-53-2)

Safety Data

• Hazardous Substances Data: 97589-53-2(Hazardous Substances Data)

Upstream product

• 56236-38-5 N-trifluoroacetyl-L-valyl chloride 
• 71-43-2 benzene 
• 349-00-8 N-trifluoroacetyl-L-valine 
• 28635-62-3 (S)-2,5-dioxopyrrolidin-1-yl 3-methyl-2-(2,2,2-trifluoroacetamido)butanoate 
• 72-18-4 L-valine 

Downstream Products

• 274686-27-0 (2S)-2-amino-3-methyl-1-phenylbutan-1-ol 

Relevant articles and documents

Synthesis of chiral TFA-protected α-amino aryl-ketone derivatives with friedel-crafts acylation of α-amino acid n-hydroxysuccinimide ester

Chiral N-protected α-amino aryl-ketones are one of the useful precursors used in the synthesis of various biologically active compounds and can be constructed via Friedel-Crafts acylation of N-protected α-amino acids. One of the drawbacks of this reaction