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CAS 176763-62-5

(R,R)-N,N'-Bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediaminocobalt(II) TCI B5732

(R,R)-N,N'-Bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediaminocobalt(II) TCI B5732

Chemical Identity

Other names
(R,R)-Co(salen) · [[2,2'-[(1R,2R)-1,2-Cyclohexanediylbis[(nitrilo-kappaN)methylidyne]]bis(4,6-di-tert-butylphenolato-kappaO)]]cobalt
CAS No.
176763-62-5
PubChem
CID 135407637
Formula
C36H52CoN2O2
Molecular weight
603.76 g/mol
Purity
>95.0%(T)
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
cobalt;2,4-ditert-butyl-6-[[(1R,2R)-2-[(3,5-ditert-butyl-2-hydroxyphenyl)methylideneamino]cyclohexyl]iminomethyl]phenol
SMILES
CC(C)(C)C1=CC(=C(C(=C1)C(C)(C)C)O)C=NC2CCCCC2N=CC3=C(C(=CC(=C3)C(C)(C)C)C(C)(C)C)O.[Co]
InChIKey
PCZWNUHBFITYKI-GAQUOPITSA-N
MDL
MDL01631277
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(R,R)-N,N'-Bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediaminocobalt(II) is a cobalt(II) salen complex commonly referred to as a Jacobsen-type catalyst, widely employed in C–H activation reactions and asymmetric catalysis. This chiral catalyst facilitates direct functionalization of unactivated carbon–hydrogen bonds and is also effective in enantioselective epoxidation and epoxide ring-opening reactions. It is a valuable reagent for synthetic organic chemistry laboratories working on pharmaceutical intermediates and fine chemical synthesis.

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