≥99.5% metals basis for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at 2-8°C,Protected from light,Argon charged Ships Wet ice 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 13 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Catalyst for [2+2+2] cycloaddtion of didehydrotriphenylenes to the corresponding extended triphenylenes. Catalyst for the carbonylation of β,β-imidoyl iodides to the corresponding imidate esters used, in turn, to prepare cyclic, quaternary amino acids. Catalyst for cross-coupling reactions.
A cycloaddition catalyst.
Product class
M-C, Homogeneous Catalysts, Diene/Dienyl Ligands
Reaction type
Cross Coupling Reactions with Arenes, Amination, Buchwald-Hartwig Aminaton, Carbonylation, Mizoroki Heck Coupling Reaction, Stille Reaction, Suzuki-Miyaura Coupling Reaction, Oxidation, Reduction
Chemical properties
C51H42O3Pd2
[Pd2(dba)3] x dba
915.73
Pd
16
crystalline
dark purple
99.95
Applications & references
Palladium catalyzed conversion of aryl chlorides and triflates to nitroaromatics.
Reference: J. Am. Chem. Soc. 2009, 131, 12898 (DOI: 10.1021/ja905768k)
Site selective sp³ palladium catalyzed direct arylation for a rapid derivatization of heterocyclic compounds.
Reference: J. Am. Chem. Soc. 2008, 130, 3266. (DOI: 10.1021/ja710451s)
One-pot ketoindoline synthesis by Palladium catalyzed γ-arylation of β,γ-unsaturated ketones.
Reference: Angew. Chem. Int. Ed. 2008, 47, 177. (DOI: 10.1002/anie.200704529)
Asymmetric synthesis of indolines by Palladium catalyzed arylation of β,γ-unsaturated ketones.
Reference: Angew. Chem. Int. Ed. 2008, 47, 177. (DOI: 10.1002/anie.200704529)
Suzuki cross coupling of aryl chorides with arylboronic acids.
Reference: Angew. Chem. Int. Ed. 1998, 37, 3387. (DOI: 10.1002/(SICI)1521-3773(19981231)37:24<3387::AID-ANIE3387>3.0.CO;2-P)
Efficient method for Suzuki-Miyaura reaction of lithium triisopropyl 2-pyridylborates and aryl chlorides.
Reference: Angew. Chem. Int. Ed. 2008, 48, 4695. (DOI: 10.1002/anie.200801465)
Palladium catalyzed aminocarbonylation of aryl halides.
Reference: J. Am. Chem. Soc. 2013, 135, 16841. (DOI: 10.1021/ja4098093)
| Sonrisas canónicas | C1=CC=C(C=C1)C=CC(=O)C=CC2=CC=CC=C2.C1=CC=C(C=C1)C=CC(=O)C=CC2=CC=CC=C2.C1=CC=C(C=C1)C=CC(=O)C=CC2=CC=CC=C2.[Pd].[Pd] |
|---|---|
| IUPAC Name | (1E,4E)-1,5-diphenylpenta-1,4-dien-3-one;palladium |
| InChIKey | CYPYTURSJDMMMP-WVCUSYJESA-N |
| INCHI | 1S/3C17H14O.2Pd/c3*18-17(13-11-15-7-3-1-4-8-15)14-12-16-9-5-2-6-10-16;;/h3*1-14H;;/b3*13-11+,14-12+;; |
| Isómeros SMILES | C1=CC=C(C=C1)/C=C/C(=O)/C=C/C2=CC=CC=C2.C1=CC=C(C=C1)/C=C/C(=O)/C=C/C2=CC=CC=C2.C1=CC=C(C=C1)/C=C/C(=O)/C=C/C2=CC=CC=C2.[Pd].[Pd] |
| WGK Alemania | 2 |
| CAS alternativo | 51364-51-3,60748-47-2 |
| Número ONU | 3077 |
| Grupo de embalaje | III |
| Peso molecular | 915.74 |
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 | Phenylpropanoids and polyketides |
| Clase | Cinnamic acids and derivatives |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Cinnamic acids and derivatives |
| Alternative Parents | Styrenes Enones Acryloyl compounds Ketones Organic transition metal salts Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Not available |
| Substituents | Cinnamic acid or derivatives - Styrene - Benzenoid - Monocyclic benzene moiety - Alpha,beta-unsaturated ketone - Enone - Acryloyl-group - Ketone - Organic transition metal salt - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aromatic homomonocyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as cinnamic acids and derivatives. These are organic aromatic compounds containing a benzene and a carboxylic acid group (or a derivative thereof) forming 3-phenylprop-2-enoic acid. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Fecha | Articulo |
|---|---|---|---|
 E2611092 | Certificate of Analysis | Aug 08, 2025 | T684863 |
| H2501586 | Certificate of Analysis | Aug 08, 2025 | T684863 |
| H2501587 | Certificate of Analysis | Aug 08, 2025 | T684863 |
| A2506367 | Certificate of Analysis | Jan 15, 2025 | T684863 |
| A2506529 | Certificate of Analysis | Jan 15, 2025 | T684863 |
| A2506538 | Certificate of Analysis | Jan 15, 2025 | T684863 |
| C2603102 | Certificate of Analysis | Jan 15, 2025 | T684863 |
| Solubilidad | Soluble in water (reacts), chloroform, DMSO (11 mM), benzene, and toluene. |
|---|---|
| Sensibilidad | Air & Moisture & light Sensitive |
| Punto de fusión (°C) | 152-155°C |
| Peso molecular | 915.700 g/mol |
| XLogP3 | |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 12 |
| Exact Mass | 916.121 Da |
| Monoisotopic Mass | 914.12 Da |
| Topological Polar Surface Area | 51.200 Ų |
| Heavy Atom Count | 56 |
| Formal Charge | 0 |
| Complexity | 272.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 6 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 6 |
| Covalently-Bonded Unit Count | 5 |
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| 5. Yongjia Lou, Jialin Xu, Luyan Xu, Zhuo Chen, Bo-Lin Lin. (2022) Chemically Recyclable CO2-Based Solid Polyesters with Facile Property Tunability. MACROMOLECULAR RAPID COMMUNICATIONS, 43 (20): (2200341). [PMID:35611450] [10.1002/marc.202200341] |
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| 7. S. B. Tan, Y. F. Zhao, W. W. Zhang, P. Gao, W. W. Zhu, Z. C. Zhang. (2017) A light-mediated metal-free atom transfer radical chain transfer reaction for the controlled hydrogenation of poly(vinylidene fluoride-chlorotrifluoroethylene). Polymer Chemistry, 9 (2): (221-227). [PMID:] [10.1039/C7PY01870C] |
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| 9. Tong Hu, Liangliang Han, Manjun Xiao, Xichang Bao, Ting Wang, Mingliang Sun, Renqiang Yang. (2014) Enhancement of photovoltaic performance by increasing conjugation of the acceptor unit in benzodithiophene and quinoxaline copolymers. Journal of Materials Chemistry C, 2 (38): (8047-8053). [PMID:] [10.1039/C4TC01440E] |
| 10. Ya Chu, Fei Zhao, Fanpeng Meng, Weiqiang Zhang, Jinsheng Zhao, Xiujuan Zhong. (2024) Donor-acceptor type conjugated porous polymers based on benzotrithiophen and triazine derivatives: Effect of linkage unit on photocatalytic water splitting. INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, [PMID:] [10.1016/j.ijhydene.2024.03.260] |
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