1020665-73-9

Basic information

• Product Name: N-[(1R,2R)-2-[[[[(1R,2R)-2-(diMethylaMino)cyclohexyl]aMino]thioxoMethyl]aMino]-1,2-diphenylethyl]-3,5-bis(trifluoroMethyl)-BenzenesulfonaMide
• Synonyms: N-[(1R,2R)-2-[[[[(1R,2R)-2-(diMethylaMino)cyclohexyl]aMino]thioxoMethyl]aMino]-1,2-diphenylethyl]-3,5-bis(trifluoroMethyl)-BenzenesulfonaMide;N-((1R,2R)-2-(3-((1R,2R)-2-(Dimethylamino)cyclohexyl)thioureido)-1,2-diphenylethyl)-3,5-bis(trifluoromethyl)benzenesulfonamide;N-[(1R,2R)-2-[[[[(1R,2R)-2-(Dimethylamino)cyclohexyl]amino]thioxomethyl]amino]-1,2-diphenylethyl]-3,5-bis(trifluoromethyl)benzenesulfonamide,99%e.e.
• CAS NO: 1020665-73-9
• Molecular Formula: C₃₁H₃₄F₆N₄O₂S₂
• Molecular Weight: 672.7476792
• Mol File: 1020665-73-9.mol
• Article Data: 1

Chemical Properties

• Melting Point: 168-170 °C
• Boiling Point: 677.5±65.0 °C(Predicted)
• Appearance: /
• Density: 1.38±0.1 g/cm3(Predicted)
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• PKA: 8.51±0.50(Predicted)
• CAS DataBase Reference: N-[(1R,2R)-2-[[[[(1R,2R)-2-(diMethylaMino)cyclohexyl]aMino]thioxoMethyl]aMino]-1,2-diphenylethyl]-3,5-bis(trifluoroMethyl)-BenzenesulfonaMide(CAS DataBase Reference)
• NIST Chemistry Reference: N-[(1R,2R)-2-[[[[(1R,2R)-2-(diMethylaMino)cyclohexyl]aMino]thioxoMethyl]aMino]-1,2-diphenylethyl]-3,5-bis(trifluoroMethyl)-BenzenesulfonaMide(1020665-73-9)
• EPA Substance Registry System: N-[(1R,2R)-2-[[[[(1R,2R)-2-(diMethylaMino)cyclohexyl]aMino]thioxoMethyl]aMino]-1,2-diphenylethyl]-3,5-bis(trifluoroMethyl)-BenzenesulfonaMide(1020665-73-9)

Safety Data

• Hazardous Substances Data: 1020665-73-9(Hazardous Substances Data)

Usage

Uses

N-((1R,2R)-2-(3-((1R,2R)-2-(Dimethylamino)cyclohexyl)thioureido)-1,2-diphenylethyl)-3,5-bis(trifluoromethyl)benzenesulfonamide functions as a chiral bifunctional organocatalyst in asymmetric synthesis.

Upstream product

• 1020665-66-0 (1R,2R)-2-isothiocyanato-N,N-dimethylcyclohexanamine 

Relevant articles and documents

Chiral amine-thioureas bearing multiple hydrogen bonding donors: Highly efficient organocatalysts for asymmetric Michael addition of acetylacetone to nitroolefins

New bifunctional organocatalysts amine-thioureas bearing multiple hydrogen bonding donors were synthesized and applied in catalytic asymmetric Michael addition of acetylacetone to aryl and alkyl nitroolefins. Multiple hydrogen bonding donors play a signif