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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Cobalt,[[3,3'-[[(1S,2S)-1,2-bis(2,4,6-trimethylphenyl)-1,2-ethanediyl]bis[(nitrilo-kN)methylidyne]]bis[2,4-pentanedionato-kO]](2-)]-, (SP-4-2)-

Cc1cc(C)c(c(c1)C)[C@@H]([C@H](c1c(C)cc(cc1C)C)/N=C/C(=C(/C)[O-])/C(=O)C)/N=C/C(=C(/C)[O-])/C(=O)C.[Co+2] Request for Quotation
Chemical Name: Cobalt,[[3,3'-[[(1S,2S)-1,2-bis(2,4,6-trimethylphenyl)-1,2-ethanediyl]bis[(nitrilo-kN)methylidyne]]bis[2,4-pentanedionato-kO]](2-)]-, (SP-4-2)-
CAS Number: 259259-80-8
Product Number: AG002R36(AGN-PC-0R1T8G)
Synonyms:
MDL No:
Molecular Formula: C32H38CoN2O4
Molecular Weight: 573.5883

Identification/Properties

Properties
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
575.615g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
4
Exact Mass:
575.232g/mol
Monoisotopic Mass:
575.232g/mol
Topological Polar Surface Area:
99.3A^2
Heavy Atom Count:
39
Formal Charge:
0
Complexity:
883
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


(1S,2S)-N,N'-Bis(2-acetyl-3-oxo-2-butenylidene)-1,2-dimesitylethylenediaminato cobalt(II) is a versatile organometallic complex that finds wide application in chemical synthesis. This cobalt complex serves as an effective catalyst in various organic transformations, including cross-coupling reactions, cycloadditions, and asymmetric transformations. Its unique chiral ligand structure imparts excellent selectivity and efficiency in promoting a range of synthetic reactions. Furthermore, its well-defined coordination environment allows for precise control over the catalytic process, leading to high yields and enantioselectivities in the products obtained. Whether utilized in the pharmaceutical industry for the synthesis of bioactive compounds or in academic research for developing novel synthetic methodologies, this cobalt complex plays a crucial role in advancing the field of organic chemistry.