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  2. Ruthenate(4-),bis[[2,2'-bipyridine]-4,4'-dicarboxylato(2-)-kN1,kN1']bis(thiocyanato-kN)-, tetrahydrogen, (OC-6-21)-

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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)-

Ruthenate(4-),bis[[2,2'-bipyridine]-4,4'-dicarboxylato(2-)-kN1,kN1']bis(thiocyanato-kN)-, tetrahydrogen, (OC-6-21)-

OC(=O)c1ccnc(c1)c1nccc(c1)C(=O)O.OC(=O)c1ccnc(c1)c1nccc(c1)C(=O)O.[N-]=C=S.[N-]=C=S.[Ru+2].[Ru+2] Request for Quotation
Chemical Name: Ruthenate(4-),bis[[2,2'-bipyridine]-4,4'-dicarboxylato(2-)-kN1,kN1']bis(thiocyanato-kN)-, tetrahydrogen, (OC-6-21)-
CAS Number: 141460-19-7
Product Number: AG009DMZ(AGN-PC-0PQUHY)
Synonyms:
MDL No:
Molecular Formula: C26H16N6O8Ru2S2++
Molecular Weight: 806.7106

Identification/Properties

Computed Properties
Molecular Weight:
705.638g/mol
Hydrogen Bond Donor Count:
4
Hydrogen Bond Acceptor Count:
16
Rotatable Bond Count:
6
Exact Mass:
705.951g/mol
Monoisotopic Mass:
705.951g/mol
Topological Polar Surface Area:
267A^2
Heavy Atom Count:
43
Formal Charge:
0
Complexity:
374
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
5
Compound Is Canonicalized:
No

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


The cis-Bis(isothiocyanato)bis(2,2′-bipyridyl-4,4′-dicarboxylato)ruthenium(II) complex is widely utilized in chemical synthesis as a versatile catalyst. This complex has been found to exhibit excellent catalytic activity in various organic transformations, such as C-C and C-N bond formation reactions. Its unique coordination environment enables the selective activation of specific functional groups, leading to high yields and efficient conversion of substrates. Additionally, the complex's stability and reactivity under mild reaction conditions make it a valuable tool in the synthesis of complex organic molecules with desired stereochemistry. By leveraging the catalytic properties of cis-Bis(isothiocyanato)bis(2,2′-bipyridyl-4,4′-dicarboxylato)ruthenium(II), chemists can streamline synthetic routes, enhance reaction selectivity, and expedite the assembly of structurally intricate compounds.