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13820-53-6 molecular structure
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palladium(2+) ion disodium tetrachloride

ChemBase ID: 302853
Molecular Formular: Cl4Na2Pd
Molecular Mass: 294.21154
Monoisotopic Mass: 291.75843528
SMILES and InChIs

SMILES:
[Na+].[Na+].[Cl-].[Cl-].[Cl-].[Cl-].[Pd+2]
Canonical SMILES:
[Na+].[Na+].[Cl-].[Cl-].[Cl-].[Cl-].[Pd+2]
InChI:
InChI=1S/4ClH.2Na.Pd/h4*1H;;;/q;;;;2*+1;+2/p-4
InChIKey:
ZIXLZKBNIAXVBE-UHFFFAOYSA-J

Cite this record

CBID:302853 http://www.chembase.cn/molecule-302853.html

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NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
IUPAC name
palladium(2+) ion disodium tetrachloride
IUPAC Traditional name
palladium(2+) ion disodium tetrachloride
Synonyms
Sodium chloropalladate(II)
Palladium sodium chloride
Sodium tetrachloropalladate(II) hydrate
四氯钯酸钠水合物
CAS Number
13820-53-6
EC Number
237-502-6
MDL Number
MFCD00003487

DATA SOURCES

DATA SOURCES

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Data Source Data ID
Alfa Aesar 11886 external link Add to cart
Data Source Data ID Price
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Data Source Data ID

CALCULATED PROPERTIES

CALCULATED PROPERTIES

JChem
Acid pKa 3.09  H Acceptors
H Donor LogD (pH = 5.5) -0.77 
LogD (pH = 7.4) -0.77  Log P -0.77 
Molar Refractivity 0.0 cm3 Polarizability 2.0172503 Å3
Polar Surface Area 0.0 Å2 Rotatable Bonds
Lipinski's Rule of Five true 

PROPERTIES

PROPERTIES

Physical Property Safety Information Product Information Bioassay(PubChem)
Apperance
Crystalline expand Show data source
Storage Warning
Hygroscopic expand Show data source
RTECS
RT3480000 expand Show data source
European Hazard Symbols
X expand Show data source
Risk Statements
22-41 expand Show data source
Safety Statements
26-36/39-60 expand Show data source
TSCA Listed
expand Show data source
GHS Pictograms
GHS05 expand Show data source
GHS07 expand Show data source
GHS Hazard statements
H318-H290-H302 expand Show data source
GHS Precautionary statements
P280F-P305+P351+P338 expand Show data source
Purity
99.95% (metals basis), Pd 30% expand Show data source

DETAILS

DETAILS

REFERENCES

REFERENCES

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  • • For use as a catalyst in the carbonylation of allylic halides to give ?-unsaturated esters, see: Chem. Lett., 1873 (1989).
  • • In the presence of CsF in aqueous MeOH, catalyzes the cross-coupling of aryl boronates with aryldiazonium salts to give biaryls; no reaction occurs in anhydrous solvents: Tetrahedron Lett., 41, 6271 (2000).
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PATENTS

PATENTS

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INTERNET

INTERNET

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