This compound is a zinc-coordinated Schiff base complex, featuring a chiral cyclohexane-1,2-diamine backbone and sterically hindered tert-butyl-substituted phenolate rings. It is primarily utilized as a research reagent in coordination chemistry and catalysis studies.
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CAS 556053-31-7
(S)-(+)-N,N-Dimethyl-1-((R)-2-(diphenylphosphino)ferrocenyl)ethylamine
chiral ligand for asymmetric catalysis
Dibromoboron;methylsulfanylmethane
Boron dibromide methyl sulfide complex
3-Acetyl-2-chloropyridine
Research chemical intermediate
Methyl 2-(11-oxo-6,11-dihydrodibenzo[b,e]oxepin-2-yl)acetate
research compound
Aluminum, chloro[[2,2'-[(1S,2S)-1,2-cyclohexanediylbis[(nitrilo-kappaN)methylidyne]]bis[4,6-bis(1,1-dimethylethyl)phenolato-kappaO]](2-)]-, (SP-5-13)-
asymmetric synthesis catalyst
(T-4)-[[2,2'-[(1R,2R)-1,2-Cyclohexanediylbis[(nitrilo-|EN)methylidyne]]bis[4,6-bis(1,1-dimethylethyl)phenolato-|EO]](2-)]zinc
research reagent
zinc 2,4-ditert-butyl-6-[[(1S,2S)-2-[(3,5-ditert-butyl-2-oxidophenyl)methylideneamino]cyclohexyl]iminomethyl]phenolate
KMUJCMSUODEDEM-PNHSAAKESA-L
CC(C)(C)C1=CC(=C(C(=C1)C(C)(C)C)[O-])C=N[C@H]2CCCC[C@@H]2N=CC3=C(C(=CC(=C3)C(C)(C)C)C(C)(C)C)[O-].[Zn+2]
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