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Dichloro(1,5-cyclooctadiene)platinum(II)

Catalog Number
ACM12080329
Product Name
Dichloro(1,5-cyclooctadiene)platinum(II)
Structure
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CAS
12080-32-9
  • Product Overview
  • Usage
Synonyms
AN-10895; 080D329; C8H12Cl2Pt; BP-12163; ST24046481; dichloroplatinum; DICHLORO(1,5-CYCLOOCTADIENE)PLATINATE (II); Pt(COD)Cl2; (1,5-Cyclooctadiene)platinum dichloride; SCHEMBL691713;
IUPAC Name
(1Z,5Z)-cycloocta-1,5-diene;dichloroplatinum;
Molecular Weight
374.18
Molecular Formula
C8H12Cl2Pt
Canonical SMILES
C1CC=CCCC=C1.Cl[Pt]Cl;
InChI
InChI=1S/C8H12.2ClH.Pt/c1-2-4-6-8-7-5-3-1;;;/h1-2,7-8H,3-6H2;2*1H;/q;;;+2/p-2/b2-1-,8-7-;;;;
InChI Key
VVAOPCKKNIUEEU-PHFPKPIQSA-L;
Purity
Metal purity 99.95
Appearance
white
Color Form
crystalline
Complexity
75.4
Covalently-Bonded Unit Count
2
Defined Bond Stereocenter Count
2
EC Number
235-144-5
Empirical Formula
[Pt(cod)Cl2]
Exact Mass
372.996g/mol
Heavy Atom Count
11
Metal Content
52
Monoisotopic Mass
372.996g/mol
Topological Polar Surface Area
0A^2
Application
Dichloro(1,5-cyclooctadiene)platinum(II) serves as a versatile catalyst, appearing as a white to pale yellow compound, primarily utilized in hydrosilylation reactions. Its efficacy extends to facilitating hydrogenative cyclization of allenynes, enabling stereoselective tandem hydrosilylation-Hiyama coupling reactions, and promoting amino alkene cyclohydroamination. Additionally, it plays a crucial role in hydrative cyclization reactions and the direct amination of allylic alcohols under mild conditions. Notably, this compound also holds potential as an anticancer agent.
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