1332828-01-9

Basic information

• Product Name: (S)-2,2,2-trifluoro-N-(4-phenylbutan-2-yl)acetamide
• Synonyms: (S)-2,2,2-trifluoro-N-(4-phenylbutan-2-yl)acetamide
• CAS NO: 1332828-01-9
• Molecular Weight: 245.244
• Mol File: 1332828-01-9.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (S)-2,2,2-trifluoro-N-(4-phenylbutan-2-yl)acetamide(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-2,2,2-trifluoro-N-(4-phenylbutan-2-yl)acetamide(1332828-01-9)
• EPA Substance Registry System: (S)-2,2,2-trifluoro-N-(4-phenylbutan-2-yl)acetamide(1332828-01-9)

Safety Data

• Hazardous Substances Data: 1332828-01-9(Hazardous Substances Data)

Upstream product

• 83167-23-1 Benzyl-[1-methyl-3-phenyl-prop-(E)-ylidene]-amine 
• 73839-93-7 1-methyl-3-phenylpropylamine hydrochloride 
• 68164-04-5 N-benzyl-1-methyl-3-phenylpropylamine 
• 22374-89-6 (RS)-1-methyl-3-phenylpropylamine 
• 407-25-0 trifluoroacetic anhydride 
• 2550-26-7 4-Phenyl-2-butanone 
• 685-27-8 2,2,2-trifluoro-N-methyl-N-(2,2,2-trifluoroacetyl)acetamide 
• 4187-57-9 (S)-1-methyl-3-phenylpropylamine 

Relevant articles and documents

Sequential reductive amination-hydrogenolysis: A one-pot synthesis of challenging chiral primary amines

Difficult-to-access chiral primary amines were formed in good to high yield and ee using a rare example of a one-pot synthesis from prochiral ketones (sequential reductive amination-hydrogenloysis). As a highlight we also demonstrate a one-pot reductive amination-hydrogenolysis-reductive amination (five reactions) of ortho-methoxyacetophenone resulting in the chiral diamine 1-(2-methoxyphenyl)ethyl-(2-pyridylmethyl)-amine (4) (58% overall yield, >99% ee), a new organocatalyst for aqueous enantioselective aldol reactions. Copyright