ChemicalBook--->CAS DataBase List--->172138-95-3

172138-95-3

172138-95-3 Structure

172138-95-3 Structure
IdentificationBack Directory
[Name]

(+)-N,N'-(1S,2S)-1,2-DIAMINOCYCLOHEXANEDIYLBIS(2-PYRIDINECARBOXAMIDE)
[CAS]

172138-95-3
[Synonyms]

(S,S)-DACH-pyridyl Trost ligand
(S,S)-DACH-pyridyl Trost ligand 95%
2,6-Bis[(4S)-benzyl-2-oxazolin-2-yl]-pyridine
N,N'-((1S,2S)-Cyclohexane-1,2-diyl)dipicolinaMide
(1S,2S)-1,2-Bis(2-pyridinecarboxamido)cyclohexane
N-((1S,2S)-2-(picolinamido)cyclohexyl)picolinamide
(1R,2R)-(-)-1,2-Bis[(2-pyridinylcarbonyl)amino]cyclohexane
1S,2S- N,N’-1,2-Diaminocyclohexanediylbis (2-pyridinecarboxamide)
(+)-N,N'-(1S,2S)-1,2-DIAMINOCYCLOHEXANEDIYLBIS(2-PYRIDINECARBOXAMIDE)
(+)-N,N'-(1S,2S)-1,2-Diaminocyclohexanediylbis(2-pyridinecarboxamide),98%
(1S,2S)-N,N'-1,2-Diaminocyclohexanediylbis(2- pyridinecarboxamide),99%e.e.
(+)-N,N'-(1S,2S)-1,2-Diaminocyclohexanediylbis(2-pyridinecarboxamide),min.98%
(+)-N,N''-(1S,2S)-1,2-DIAMINOCYCLOHEXANEDIYLBIS(2-PYRIDINECARBOXAMIDE), MIN. 98%
(1R,2R)-N,Nμ-1,2-Cyclohexanediylbis(2-pyridinecarboxamide), (1R,2R)-1,2-Bis(2-pyridinecarboxamido)cyclohexane
(+)-N,N'-(1S,2S)-1,2-Diaminocyclohexanediylbis(2-pyridinecarboxamide), min. 98% (S,S)-DACH-Pyridyl Trost Ligand
(1S,2S)-N,Nμ-1,2-Cyclohexanediylbis(2-pyridinecarboxamide), (+)-N,Nμ-(1S,2S)-1,2-Diaminocyclohexanediylbis(2-pyridinecarboxamide), (1S,2S)-(+)-1,2-Bis[(2-pyridinylcarbonyl)amino]cyclohexane, (1S,2S)-1,2-Bis(2-pyridinecarboxamido)cyclohexane
[Molecular Formula]

C18H20N4O2
[MDL Number]

MFCD02684544
[MOL File]

172138-95-3.mol
[Molecular Weight]

324.38
Chemical PropertiesBack Directory
[Melting point ]

170°C
[alpha ]

+95° (c 1, CH3OH)
[storage temp. ]

2-8°C
[form ]

Powder
[color ]

off-white
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[Hazard Codes ]

Xn
[Risk Statements ]

36/37/38-22
[Safety Statements ]

26-36/37/39-36/37
Questions And AnswerBack Directory
[Reactions]

  1. Ligands for Mo catalyzed asymmetric allylic substitutions. Especially useful for the synthesis of tertiary and quaternary stereocenters. Exclusive license for this technology acquired by ChiroTech and is protected by pending Stanford University patents.
  2. Dynamic kinetic asymmetric formation of tertiary and quaternary stereogenic centers
Reactions of 172138-95-3
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