91994-60-4

Basic information

• Product Name: Acetamide, 2,2,2-trifluoro-N-(2-hydroxy-2-phenylethyl)-
• CAS NO: 91994-60-4
• Molecular Formula: C10H10F3NO2
• Molecular Weight: 233.19
• Mol File: 91994-60-4.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: Acetamide, 2,2,2-trifluoro-N-(2-hydroxy-2-phenylethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Acetamide, 2,2,2-trifluoro-N-(2-hydroxy-2-phenylethyl)-(91994-60-4)
• EPA Substance Registry System: Acetamide, 2,2,2-trifluoro-N-(2-hydroxy-2-phenylethyl)-(91994-60-4)

Safety Data

• Hazardous Substances Data: 91994-60-4(Hazardous Substances Data)

Upstream product

• 100-42-5 styrene 
• 1337984-76-5 1-(2,2,2-trifluoroacetylimino)pyridinium ylide 
• 5468-37-1 2-aminoacetophenone hydrochloride 
• 407-25-0 trifluoroacetic anhydride 
• 91994-49-9 2,2,2-trifluoro-N-(2-oxo-2-phenylethyl)acetamide 
• 96-09-3 styrene oxide 
• 354-38-1 2,2,2-trifluoroacetamide 

Downstream Products

• 7568-93-6 2-Amino-1-phenylethanol 

Relevant articles and documents

Pyrazolone-based nitrido complexes: Synthesis and nitrogen transfer to alkenes

The first examples of alkylpyrazolone based nitridomanganese(v) complexes are here reported. Styrene was used as a test substrate to study the complex's ability to transfer nitrogen in stoichiometric reactions. Preliminary trials yielded 75 to 91% of N-(2

Regioselective opening of epoxides to β-amido alcohols under solid-liquid PTC conditions

A study on the ring opening of a number of epoxides 1 with trifluoroacetamide (2) under solid-liquid phase transfer catalysis (SL-PTC) conditions has been performed. The reaction is completely regioselective affording β-amido alcohols 3 deriving from the attack of the nucleophile to the less substituted carbon atom of the oxirane ring.

Baker's Yeast Reduction of α-(Acylamino)acetophenones and Lipase Catalyzed Resolution of 2-Acylamino-1-arylethanols

Enzymatic reduction of α-acylaminoacetophenones with fermenting baker's yeast afforded optically active (R)-2-acylamino-1-arylethanols.Furthermore, lipase-catalyzed resolution of the 2-acylamino-1-arylethanols using vinyl acetate as an acyl donor resulted in the formation of (S)-1-acetoxy-2-acylamino-1-arylethanols and (R)-2-acylamino-1-arylethanols.