35963-83-8

Basic information

• Product Name: dichloroplatinum(2+) 4-chloropiperidin-1-ide 4-chloro-2H-pyridin-1-ide (1:1:1)
• CAS NO: 35963-83-8
• Molecular Formula: C₁₀H₁₄Cl₄N₂Pt
• Molecular Weight: 499.1276
• Mol File: 35963-83-8.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 173.8°C at 760 mmHg
• Flash Point: 58.9°C
• Vapor Pressure: 1.24mmHg at 25°C
• CAS DataBase Reference: dichloroplatinum(2+) 4-chloropiperidin-1-ide 4-chloro-2H-pyridin-1-ide (1:1:1)(CAS DataBase Reference)
• NIST Chemistry Reference: dichloroplatinum(2+) 4-chloropiperidin-1-ide 4-chloro-2H-pyridin-1-ide (1:1:1)(35963-83-8)
• EPA Substance Registry System: dichloroplatinum(2+) 4-chloropiperidin-1-ide 4-chloro-2H-pyridin-1-ide (1:1:1)(35963-83-8)

Safety Data

• Hazardous Substances Data: 35963-83-8(Hazardous Substances Data)

Upstream product

• 626-61-9 4-Chloropyridine 
• 41276-66-8 cis-[rac-1,2-bis(phenylsulphinyl)ethane]dichloroplatinum(II) 
• 41233-57-2 cis-[meso-1,2-bis(phenylsulphinyl)ethane]dichloroplatinum(II) 
• 10025-99-7 potassium tetrachloroplatinate(II) 
• 68099-02-5 cis-tetrachlorobis(4-chloropyridine)platinum(II) 
• 68-05-3 tetraethylammonium iodide 

Downstream Products

• 68099-02-5 cis-tetrachlorobis(4-chloropyridine)platinum(II) 

Relevant articles and documents

Acid-Base Equilibria of Co-ordinated Ligands. Part 1. The Effect of Basicity of Co-ordinated Nitrogen Donors upon the Acidity of Chelating 8-Aminoquinoline in some Dicationic Platinum(II) Complexes

Cationic complexes of the type 2 and 2 (8NH2-quin = 8-aminoquinoline), where L and L-L are mono- and bi-dentate nitrogen donors respectively, have been prepared.In aqueous solution, they undergo reversible

Nucleophilic displacement of the chelating bis(sulfoxide) from cis-[meso-1,2-bis(phenylsulfinyl)ethane]dichloroplatinum(II) and cis-[rac-1,2-bis(phenylsulfinyl)ethane]dichloroplatinum(II)

The kinetics of ring opening, by amines in 1,2-dimethoxyethane, have been measured for two bis(sulfoxide)-platinum(II) isomers. The results make possible a discussion of the differences between the two isomers, in comparison with other platinum(II) complexes, in terms of absolute reactivity, nucleophilic discrimination, and steric retardation effects.