Basic information Safety Supplier Related

Epi-N-Quinyl-N’-bis(3,5-trifluoromethyl) phenylthiourea

Basic information Safety Supplier Related

Epi-N-Quinyl-N’-bis(3,5-trifluoromethyl) phenylthiourea Basic information

Product Name:
Epi-N-Quinyl-N’-bis(3,5-trifluoromethyl) phenylthiourea
Synonyms:
  • N-[3,5-Bis(trifluoromethyl)phenyl]-N'-[(8a,9S)-6'-methoxy-9-cinchonanyl]thiourea
  • N-[3,5-Bis(trifluoromethyl)phenyl]-N'-[(8a,9S)-6'-methoxy-9-cinchonanyl]thiourea 90%
  • 1-[3,5-BIS(TRIFLUOROMETHYL)PHENYL]-3-[(S)(6-METHOXY-4-QUINOLINYL)-[(2S,4S,5R)-5-VINYL-1-AZA-BICYCLO[2.2.2]OCT-2-YL]METHYL]THIOUREA
  • 1-[3,5-bis(trifluoromethyl)phenyl]-3-[(S)-[(1S,2S,4S,5R)-5-ethenyl-1-azabicyclo[2.2.2]octan-2-yl](6-methoxyquinolin-4-yl)methyl]thiourea
  • N-[3,5-Bis(trifluoromethyl)phenyl]-N'-[(8α,9S)-6'-methox ycinchonan-9-yl]thiourea,99%d.e.
  • 1-(3,5-Bis(trifluoromethyl)phenyl)-3-((6-methoxyquinolin-4-yl)((1S,2R,4S,5R)-5-vinylquinuclidin-2-yl)methyl)thiourea
  • 1-(3,5-Bis(trifluoromethyl)phenyl)-3-((S)-(6-methoxyquinolin-4-yl)((1S,2S,4S,5R)-5-vinylquinuclidin-2-yl)methyl)thiourea
  • Epi-N-Quinyl-N’-bis(3,5-trifluoromethyl) phenylthiourea
CAS:
852913-16-7
MF:
C29H28F6N4OS
MW:
594.61
Mol File:
852913-16-7.mol
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Epi-N-Quinyl-N’-bis(3,5-trifluoromethyl) phenylthiourea Chemical Properties

Boiling point:
598.2±60.0 °C(Predicted)
Density 
1.39±0.1 g/cm3(Predicted)
pka
11.39±0.70(Predicted)
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Safety Information

Hazard Codes 
T
Risk Statements 
25
Safety Statements 
45
RIDADR 
UN 2811 6.1 / PGIII
HS Code 
29339900
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Epi-N-Quinyl-N’-bis(3,5-trifluoromethyl) phenylthiourea Usage And Synthesis

Chemical Properties

Solid

Uses

N-[3,5-Bis(trifluoromethyl)phenyl]-N′-[(8a,9S)-6′-methoxy-9-cinchonanyl]thiourea is a bifunctional cinchona organocatalyst, which can be used to synthesize:

  • Stereoselective diaryl(nitro)butanone via enantioselective Michael addition of nitromethane to chalcones.
  • Enantioselective β-amino acids via asymmetric Mannich reaction of malonates with aryl and alkyl imines.
  • The synthesis of 3-indolylmethanamines by the reaction of indoles with imines via asymmetric Friedel-Crafts reaction.
  • The enantioselective conjugate addition of active methylene compounds to enones to obtain the corresponding addition products.

Epi-N-Quinyl-N’-bis(3,5-trifluoromethyl) phenylthioureaSupplier

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