Determine the necessary mass, volume, or concentration for preparing a solution.
≥99.95% metals basis for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature Ships Normal Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Application
Catalyst for:
1.Aerobic cyclization of acrylic acid with alkenes
2.Benzylation of heterocycles with benzyl chlorides
3.ntramolecular direct arylation reactions
4.Regioselective oxidative arene cross-coupling
Product class
Homogeneous Catalysts, M-O
Reaction type
C-H Activation
Chemical properties
C30H54O12Pd3
[Pd(OOCtBu)2]3
926.01
Pd
35
powder
orange
99.95
| Pubchem Sid | 329763862 |
|---|---|
| Sonrisas canónicas | CC(C)(C)C(=O)[O-].CC(C)(C)C(=O)[O-].[Pd+2] |
| IUPAC Name | 2,2-dimethylpropanoate;palladium(2+) |
| InChIKey | PAGZTSLSNQZYEV-UHFFFAOYSA-L |
| INCHI | 1S/2C5H10O2.Pd/c2*1-5(2,3)4(6)7;/h2*1-3H3,(H,6,7);/q;;+2/p-2 |
| Isómeros SMILES | CC(C)(C)C(=O)[O-].CC(C)(C)C(=O)[O-].[Pd+2] |
| WGK Alemania | 3 |
| PubChem CID | 24905427 |
| Peso molecular | 308.67 |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic acids and derivatives |
| Clase | Carboxylic acids and derivatives |
| Subclass | Carboxylic acid derivatives |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Carboxylic acid salts |
| Alternative Parents | Organic transition metal salts Monocarboxylic acids and derivatives Carboxylic acids Organic oxides Hydrocarbon derivatives Carbonyl compounds Organic cations |
| Molecular Framework | Not available |
| Substituents | Carboxylic acid salt - Organic transition metal salt - Monocarboxylic acid or derivatives - Carboxylic acid - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organic salt - Organooxygen compound - Carbonyl group - Organic cation - Aliphatic acyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as carboxylic acid salts. These are ionic derivatives of carboxylic acid. |
| External Descriptors | Not available |
| Punto de fusión (°C) | 230-232°C |
|---|---|
| Peso molecular | 308.670 g/mol |
| XLogP3 | |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 0 |
| Exact Mass | 308.024 Da |
| Monoisotopic Mass | 308.024 Da |
| Topological Polar Surface Area | 80.300 Ų |
| Heavy Atom Count | 15 |
| Formal Charge | 0 |
| Complexity | 73.100 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 3 |