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567221

Sigma-Aldrich

Tris(3,3′,3″-phosphinidynetris(benzenesulfonato)palladium(0) nonasodium salt nonahydrate

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About This Item

Linear Formula:
Pd(P(C6H4SO3·Na)3)3 · 9H2O
CAS Number:
Molecular Weight:
1982.89
MDL number:
UNSPSC Code:
12161600
PubChem Substance ID:
NACRES:
NA.22

form

solid

Quality Level

reaction suitability

core: palladium
reaction type: Buchwald-Hartwig Cross Coupling Reaction
reaction type: Cross Couplings
reaction type: Heck Reaction
reaction type: Hiyama Coupling
reaction type: Negishi Coupling
reaction type: Sonogashira Coupling
reaction type: Stille Coupling
reaction type: Suzuki-Miyaura Coupling
reagent type: catalyst

mp

>300 °C (lit.)

storage temp.

2-8°C

SMILES string

[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Pd].[H]O[H].[H]O[H].[H]O[H].[H]O[H].[H]O[H].[H]O[H].[H]O[H].[H]O[H].[H]O[H].[O-]S(=O)(=O)c1cccc(c1)P(c2cccc(c2)S([O-])(=O)=O)c3cccc(c3)S([O-])(=O)=O.[O-]S(=O)(=O)c4cccc(c4)P(c5cccc(c5)S([O-])(=O)=O)c6cccc(c6)S([O-])(=O)=O.[O-]S(=O)(=O)c7cccc(c7)P(c8cccc(c8)S([O-])(=O)=O)c9cccc(c9)S([O-])(=O)=O

InChI

1S/3C18H15O9PS3.9Na.9H2O.Pd/c3*19-29(20,21)16-7-1-4-13(10-16)28(14-5-2-8-17(11-14)30(22,23)24)15-6-3-9-18(12-15)31(25,26)27;;;;;;;;;;;;;;;;;;;/h3*1-12H,(H,19,20,21)(H,22,23,24)(H,25,26,27);;;;;;;;;;9*1H2;/q;;;9*+1;;;;;;;;;;/p-9

InChI key

RZJLWYKBARRAJM-UHFFFAOYSA-E

Application

Tris(3,3′,3″-phosphinidynetris(benzenesulfonato)palladium(0) nonasodium salt nonahydrate (Pd-TPPTS complex) supported by layered double hydroxide (LDH) can be used as an efficient catalyst in the cycloisomerization of acetylenic carboxylic acids to the corresponding 5-membered heterocycles.

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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Novel Pd heterogeneous catalysts for cycloisomerisation of acetylenic carboxylic acids
Neactu F, et al.
Green Chemistry, 12(12), 2145-2149 (2010)

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