(R,R)-(-)-N,N'-Bis(3,5-ditert-butylsalicylidene)-1,2-cyclohexanediaminocobalt(II)
CAS: 176763-62-5
Rif. 3D-FR138978
1g | Fuori produzione | ||
2g | Fuori produzione | ||
5g | Fuori produzione | ||
10g | Fuori produzione | ||
25g | Fuori produzione |
Informazioni sul prodotto
- (1R,2R)-(-)-N,N-Bis(3,5-di-t-butylsalicylidene)-1,2-cyclohexanediaminocobalt(II)
- (R,R)-()-N,N-Bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediaminocobalt(II)
- (R,R)-(-)-N,N'-Bis(3,5-Di-Tert-Butylsalicylidene)-1,2-Cyclohexanediamino-Cobalt(Ii)
- (R,R)-(-)-N,N-bis(3,5-di-T-butylsalicylid -ene)-
- (R,R)-Co(salen)
- (R,R)-Jacobsen HKR catalyst
- (R,R)-N,N′-Bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediaminatocobalt(II)
- (SP-4-2)-[[2,2′-[(1R,2R)-1,2-Cyclohexanediylbis[(nitrilo-κN)methylidyne]]bis[4,6-bis(1,1-dimethylethyl)phenolato-κO]](2-)]cobalt
- 2,2'-{(1R,2R)-cyclohexane-1,2-diylbis[nitrilo(E)methylylidene]}bis(4,6-di-tert-butylphenol)-cobalt (1:1)
- Cobalt, [[2,2′-[(1R,2R)-1,2-cyclohexanediylbis[(nitrilo-κN)methylidyne]]bis[4,6-bis(1,1-dimethylethyl)phenolato-κO]](2-)]-, (SP-4-2)-
- Vedi altri sinonimi
- Cobalt, [[2,2′-[1,2-cyclohexanediylbis(nitrilomethylidyne)]bis[4,6-bis(1,1-dimethylethyl)phenolato]](2-)-N,N′,O,O′]-, [SP-4-2-(1R-trans)]-
- Cobalt, [[2,2′-[1,2-cyclohexanediylbis[(nitrilo-κN)methylidyne]]bis[4,6-bis(1,1-dimethylethyl)phenolato-κO]](2-)]-, [SP-4-2-(1R-trans)]-
- N,N′-Bis(3,5-di-tert-butylsalicylidene)-1,2-diaminocyclohexanecobalt(II)
- [[2,2′-[(1R,2R)-1,2-Cyclohexanediylbis[(nitrilo-κN)methylidyne]]bis[4,6-bis(1,1-dimethylethyl)phenolato-κO]](2-)]cobalt
- (1R,2R)-(-)-1,2-cyclohexanediamino-N,N'-bis-(3,5-di-t-butylsalicylidene)cobalt (II)
- (1R,2R)-(-)-1,2-Cyclohexanediamino-N,N'-bis(3,5-di-t-butylsalicylidene)cobalt(II)
(R,R)-(-)-N,N'-Bis(3,5-ditert-butylsalicylidene)-1,2-cyclohexanediaminocobalt(II) is a chiral ligand that is used in asymmetric synthesis. It can be prepared by the desymmetrization of (S,S)-(-)-N,N'-bis-(3,5-ditert-butylsalicylidene)-1,2-cyclohexanediaminocobalt(II). This compound has been found to be stable and enantioselective in catalytic reactions. The compound exhibits kinetic behavior with an orange color and a red solid state.