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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)-

Platinum, dichlorobis[1,1'-thiobis[ethane]]-, (SP-4-2)-

CCSCC.CCSCC.Cl[Pt]Cl Request for Quotation
Chemical Name: Platinum, dichlorobis[1,1'-thiobis[ethane]]-, (SP-4-2)-
CAS Number: 15442-57-6
Product Number: AG003P00(AGN-PC-0Q6PRO)
Synonyms:
MDL No:
Molecular Formula: C8H20Cl2PtS2
Molecular Weight: 446.3584

Identification/Properties

Properties
MP:
105 °C(lit.);
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
446.352g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
4
Exact Mass:
445.003g/mol
Monoisotopic Mass:
445.003g/mol
Topological Polar Surface Area:
50.6A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
13.9
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:
3
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


cis-Dichlorobis(diethylsulfide)platinum(II) is a compound that serves as a valuable reagent in chemical synthesis. With its unique structure and properties, this complex is utilized in various synthetic reactions to facilitate the formation of important chemical bonds. One common application of cis-Dichlorobis(diethylsulfide)platinum(II) is in the coordination and activation of carbon-carbon double bonds, a process essential in the production of organic compounds. Additionally, this compound has been found to be effective in catalyzing cross-coupling reactions, where it promotes the coupling of different functional groups to form new carbon-carbon bonds. Its ability to selectively activate certain functional groups makes cis-Dichlorobis(diethylsulfide)platinum(II) a versatile tool in the toolkit of synthetic chemists striving to create complex molecules with precision and efficiency.