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
The following palladium dimer is a precatalyst scaffold for cross-coupling reactions originally reported by the Hazari research group. When used with an selected ligand, the precatalyst exhibits superior activity over a wide array of cross-coupling reactions and under a variety of conditions.
Product class
M-C, Homogeneous Catalysts, Hazari Catalyst, Indenyl Ligands
Reaction type
Cross Coupling Reactions with Arenes, Amination, Buchwald-Hartwig Aminaton, Suzuki-Miyaura Coupling Reaction
Chemical properties
C26H30Cl2Pd2
[Pd(1-tBu-Ind)Cl]2
626.27
Pd
34
99.95
Applications & references
Suzuki-Miyaura coupling reaction catalyzed by an in situ generated solution of [Pd(cinnamyl)Cl]2 and IPr and an in situ generated solution of our Pd-cat. and IPr.
Reference: ACS Catal. 2015, 5, 3680 (DOI: 10.1021/acscatal.5b00878)
Suzuki-Miyaura coupling reaction of 2-chloro-4,6-dimethoxyprimidine and benzofuran-2-boronic acid catalyzed by an in situ precatalyst generated from our Pd-cat. and XPhos.
Reference: ACS Catal. 2015, 5, 3680 (DOI: 10.1021/acscatal.5b00878)
Suzuki-Miyaura coupling reaction of 2-chloro-1H-benzimidazole and 3-thiophene boronic acid catalyzed by an in situ precatalyst generated from Umicore our Pd-cat. and SPhos.
Reference: ACS Catal. 2015, 5, 3680 (DOI: 10.1021/acscatal.5b00878)
Suzuki-Miyaura coupling reaction of 2-methoxy chlorobenzene and morpholine catalyzed by an in situ precatalyst generated from our Pd-cat. and RuPhos.
Reference: ACS Catal. 2015, 5, 3680 (DOI: 10.1021/acscatal.5b00878)
Suzuki-Miyaura coupling reaction of 3-acetylpyridine and 3-chloropyridine catalyzed by an in situ precatalyst generated from our Pd-cat. and XPhos.
Reference: ACS Catal. 2015, 5, 3680 (DOI: 10.1021/acscatal.5b00878)
Suzuki-Miyaura coupling reaction of 4-chloroanisole and potassium isopropyltrifluoroboronate catalyzed by an in situ precatalyst generated from our Pd-cat. and P(tBu)3.
Reference: ACS Catal. 2015, 5, 3680 (DOI: 10.1021/acscatal.5b00878)
Hiyama-Denmark Reactions of 4-(trifluoromethyl)chlorobenzene and 4-(methoxy)phenyl silanolate catalyzed by in situ precatalysts generated from our Pd-cat. and different ligands.
Reference: Org. Lett. 2016, 18, 5784 (DOI: 10.1021/acs.orglett.6b02330)
| Canonical Smiles | CC(C)(C)C1[C-]=CC2=CC=CC=C12.CC(C)(C)C1[C-]=CC2=CC=CC=C12.Cl[Pd+].Cl[Pd+] |
|---|---|
| IUPAC Name | 1-tert-butyl-1,2-dihydroinden-2-ide;chloropalladium(1+) |
| InChIKey | QRXJPFMMPGIVGO-UHFFFAOYSA-L |
| INCHI | 1S/2C13H15.2ClH.2Pd/c2*1-13(2,3)12-9-8-10-6-4-5-7-11(10)12;;;;/h2*4-8,12H,1-3H3;2*1H;;/q2*-1;;;2*+2/p-2 |
| WGK Germany | 3 |
| PubChem CID | 155885086 |
| Molecular Weight | 626.26 |
Comprehensive hazard, handling, storage, and regulatory compliance document.
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View spec sheet →| Melt Point(°C) | 166 °C |
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