Cobalt,[[2,2'-[(1,2-diphenyl-1,2-ethanediyl)bis[(nitrilo-kN)methylidyne]]bis[1-(2,4,6-trimethylphenyl)-1,3-butanedionato-kO3]](2-)]-, (SP-4-2)- (9CI)


Chemical Name: Cobalt,[[2,2'-[(1,2-diphenyl-1,2-ethanediyl)bis[(nitrilo-kN)methylidyne]]bis[1-(2,4,6-trimethylphenyl)-1,3-butanedionato-kO3]](2-)]-, (SP-4-2)- (9CI)
CAS Number: 212250-92-5
Product Number: AG003BGP(AGN-PC-0QXT25)
Synonyms:
MDL No:
Molecular Formula: C42H42CoN2O4
Molecular Weight: 697.7271

Identification/Properties


Properties
Storage:
Inert atmosphere;2-8℃;
Computed Properties
Molecular Weight:
697.741g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
11
Exact Mass:
697.248g/mol
Monoisotopic Mass:
697.248g/mol
Topological Polar Surface Area:
105A^2
Heavy Atom Count:
49
Formal Charge:
0
Complexity:
1100
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
2
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
2
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
2
Compound Is Canonicalized:
Yes

Safety Information


GHS Pictogram:
Signal Word:
Danger
UN#:
2811
Hazard Statements:
H351
Precautionary Statements:
P501-P202-P201-P280-P308+P313-P405
Class:
6.1
Packing Group:

NMR Spectrum


Other Analytical Data


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Chemical Structure



(1R,2R)-N,N'-Bis[3-oxo-2-(2,4,6-trimethylbenzoyl)butylidene]-1,2-diphenylethylenediaminato cobalt(II) is a versatile compound frequently utilized in chemical synthesis as a catalyst with remarkable asymmetric induction properties. Its structure allows for precise control over the stereochemistry of reactions, making it a valuable tool in the synthesis of chiral molecules. This cobalt complex has found particular success in promoting various organic transformations, such as asymmetric cyclopropanation, oxidation reactions, and cross-coupling reactions. Its efficiency and selectivity make it a highly sought-after reagent in the field of organic chemistry, enabling chemists to access complex molecules with high levels of stereocontrol.