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
Umicore CX231 is a homogeneous catalyst useful for cross-coupling reactions with arenes, Buchwald-Hartwig aminaton reactions, and Suzuki-Miyaura cross-couplings.
Storage and Stability
Do not store above 25°C (77°F). Store in a tightly closed original container under dry inert gas, protected from direct sunlight in a dry, cool and well-ventilated area.
Product class
M-P, Homogeneous Catalysts, M-C, Hazari Catalyst, Indenyl Ligands, Phosphorus Ligands - Achiral
Reaction type
Cross Coupling Reactions with Arenes, Amination, Buchwald-Hartwig Aminaton, Suzuki-Miyaura Coupling Reaction
Chemical properties
C40H51ClN2Pd
[(IPr)Pd(1-tBu-Ind)Cl]
701.71
Pd
15
99.95
Applications & references
Suzuki-Miyaura coupling reactions of various substrates using a weak base showing the significant outperformance of Umicore CX231 compared to Umicore CX31. The conversion of substrates with deactivating electron-donating groups and substituents in the ortho-positions is feasible.
Reference: ACS Catal. 2015, 5, 3680 (DOI: 10.1021/acscatal.5b00878)
Suzuki-Miyaura coupling reaction of both linear and cyclic alkyl trifluoroboronates salts and various aryl chlorides, including an example of a nitrogen-containing heterocycle.
Reference: ACS Catal. 2015, 5, 3680 (DOI: 10.1021/acscatal.5b00878)
Firstly reported Hiyama-Denmark reactions using aryl silanolates as nucleophiles as an alternative to Suzuki-Miyaura reactions.
Reference: Org. Lett. 2016, 18, 5784 (DOI: 10.1021/acs.orglett.6b02330)
| Sorrisos canónicos | CC(C)C1=C(C(=CC=C1)C(C)C)N2[CH-]N(C=C2)C3=C(C=CC=C3C(C)C)C(C)C.CC(C)(C)C1[C-]=CC2=CC=CC=C12.Cl[Pd+] |
|---|---|
| IUPAC Name | 1,3-bis[2,6-di(propan-2-yl)phenyl]-2H-imidazol-2-ide;1-tert-butyl-1,2-dihydroinden-2-ide;chloropalladium(1+) |
| InChIKey | NIWJLEATKKVIDN-UHFFFAOYSA-M |
| INCHI | 1S/C27H37N2.C13H15.ClH.Pd/c1-18(2)22-11-9-12-23(19(3)4)26(22)28-15-16-29(17-28)27-24(20(5)6)13-10-14-25(27)21(7)8;1-13(2,3)12-9-8-10-6-4-5-7-11(10)12;;/h9-21H,1-8H3;4-8,12H,1-3H3;1H;/q2*-1;;+2/p-1 |
| PubChem CID | 139036022 |
| Peso molecular | 701.72 |
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 →| Ponto de fusão (°C) | >300 °C |
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