313342-12-0

Basic information

• Product Name: N-[(1S,2S)-2-aMinocyclohexyl]-1,1,1-trifluoro-MethanesulfonaMide
• Synonyms: N-[(1S,2S)-2-aMinocyclohexyl]-1,1,1-trifluoro-MethanesulfonaMide
• CAS NO: 313342-12-0
• Molecular Formula: C7H13F3N2O2S
• Molecular Weight: 246.2505296
• Mol File: 313342-12-0.mol

Chemical Properties

• Boiling Point: 269.7±50.0 °C(Predicted)
• Appearance: /
• Density: 1.41±0.1 g/cm3(Predicted)
• PKA: 5.43±0.20(Predicted)
• CAS DataBase Reference: N-[(1S,2S)-2-aMinocyclohexyl]-1,1,1-trifluoro-MethanesulfonaMide(CAS DataBase Reference)
• NIST Chemistry Reference: N-[(1S,2S)-2-aMinocyclohexyl]-1,1,1-trifluoro-MethanesulfonaMide(313342-12-0)
• EPA Substance Registry System: N-[(1S,2S)-2-aMinocyclohexyl]-1,1,1-trifluoro-MethanesulfonaMide(313342-12-0)

Safety Data

• Hazardous Substances Data: 313342-12-0(Hazardous Substances Data)

Upstream product

• 1160841-06-4 benzyl (1S,2S)-2-(trifluoromethylsulfonamido)cyclohexylcarbamate 
• 358-23-6 trifluoromethylsulfonic anhydride 
• 438588-60-4 2-((1R,2R)-2-aminocyclohexyl)isoindoline-1,3-dione 

Relevant articles and documents

The effect of hydrogen bond donors in asymmetric organocatalytic conjugate additions

A series of primary amine organocatalysts with various hydrogen bond donors were prepared and examined in the conjugate addition of isobutyraldehyde and acetone to trans-β-nitrostyrene and (E)-methyl 2-oxo-4-phenylbut-3-enoate. The effect of N-H acidity a

A novel bifunctional sulfonamide primary amine-catalyzed enantioselective conjugate addition of ketones to nitroolefins

The enantioselective conjugate addition of a variety of ketones to nitroolefins has been developed. The process is efficiently catalyzed by a novel bifunctional sulfonamide primary amine in good yields and with good levels of enantioselectivity.