cis-Dichlorobis(diethyl sulfide)platinum(II)

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Catalog Number
ACM15442576-2
Product Name
cis-Dichlorobis(diethyl sulfide)platinum(II)
Structure
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CAS
15442-57-6
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Synonyms
Platinum, dichlorobis(1,1'-thiobis(ethane))-; ethylsulfanylethane; C8H20Cl2PtS2; 15442-57-6; trans-Dichlorobis(diethylsulfide)platinum(II); cis-Dichlorobis(diethylsulfide)platinum(II); 15337-84-5; CTK6G5001; Dichlorobis(1,1'-thiobis(ethane))platinum; trans-Dichlorobis(diethylsulfide)platinum(II), Pt 43.7%;
IUPAC Name
dichloroplatinum;ethylsulfanylethane;
Molecular Weight
446.352g/mol
Molecular Formula
C8H20Cl2PtS2;
Canonical SMILES
CCSCC.CCSCC.Cl[Pt]Cl;
InChI
InChI=1S/2C4H10S.2ClH.Pt/c2*1-3-5-4-2;;;/h2*3-4H2,1-2H3;2*1H;/q;;;;+2/p-2;
InChI Key
DCIVLRIRJUWCIS-UHFFFAOYSA-L;
Complexity
13.9
Covalently-Bonded Unit Count
3
EC Number
239-454-1
Exact Mass
445.003g/mol
H-Bond Acceptor
2
Heavy Atom Count
13
Monoisotopic Mass
445.003g/mol
Rotatable Bond Count
4
Topological Polar Surface Area
50.6A^2
Application
cis-Dichlorobis(diethyl sulfide)platinum(II) serves as a versatile chemical reagent pivotal in the preparation of various platinum compounds. This colorless solid, with a melting point of 173°C, plays a crucial role in the synthesis of benzenesulfonyl chloride and benzene. These substances are key intermediates in the pharmaceutical industry, particularly in the production of important drugs such as carbapenems and fluoroquinolones. Furthermore, cis-Dichlorobis(diethyl sulfide)platinum(II) undergoes an isomerization reaction with agents like lithium, ether, or sulfide to produce cis-Dichlorobis(ethyl sulfide)platinum(II), showcasing its capability in facilitating complex chemical transformations.
April 6, 2025

Highly Effective Reagent for Platinum Compound Synthesis

Cis-Dichlorobis(diethyl sulfide)platinum(II) efficiently supports our synthesis of pharmaceutical intermediates. Its reliability and ease of use enhance our research outcomes in developing essential drugs. Highly recommend for industrial chemical synthesis.

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