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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)-

Dimethylammoniumdichlorotri(mu-chloro)bis[(S)-(-)-2,2’-bis(di-p-tolylphosphino)-1,1’-binaphthyl]diruthenate(II)

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Chemical Name: Dimethylammoniumdichlorotri(mu-chloro)bis[(S)-(-)-2,2’-bis(di-p-tolylphosphino)-1,1’-binaphthyl]diruthenate(II)
CAS Number: 309735-86-2
Product Number: AG0031SK(AGN-PC-0R6DJ5)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

Identification/Properties

Properties
MP:
>100℃
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
1783.074g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
14
Exact Mass:
1786.241g/mol
Monoisotopic Mass:
1781.24g/mol
Topological Polar Surface Area:
12A^2
Heavy Atom Count:
110
Formal Charge:
0
Complexity:
902
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:
6
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


Dimethylammonium Dichlorotri(μ-chloro)bis[(S)-(-)-2,2-bis(di-p-tolylphosphino)-1,1-binaphthyl]diruthenate(II) is a versatile catalyst commonly used in chemical synthesis. This complex plays a crucial role in promoting various organic transformations due to its unique structure and reactivity.In organic chemistry, this compound is often employed in asymmetric catalysis reactions, where it facilitates the formation of chiral compounds with high enantioselectivity. Its ability to selectively activate certain functional groups and control the stereochemistry of the reaction makes it an essential tool for synthesizing complex molecules with desired optical properties.Moreover, Dimethylammonium Dichlorotri(μ-chloro)bis[(S)-(-)-2,2-bis(di-p-tolylphosphino)-1,1-binaphthyl]diruthenate(II) is known for its stability under a wide range of reaction conditions, making it suitable for use in both aqueous and organic solvents. Additionally, its high catalytic activity and low catalyst loading requirement contribute to its cost-effectiveness and practicality in large-scale synthesis processes.Overall, this catalyst represents a valuable asset in the toolkit of synthetic chemists seeking efficient and selective methods for the preparation of enantiomerically enriched compounds in both academic research and industrial applications.