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CAS RN: 113173-22-1 | Product Number: B5400
Bis(1,10-phenanthroline)palladium(II) Bis(hexafluorophosphate)
Purity: >98.0%(T)
Synonyms:
Product Documents:
Size | Unit Price | Belgium | Japan* | Quantity |
---|---|---|---|---|
200MG |
122,00 €
|
1 | 7 |
|
1G |
389,00 €
|
1 | 28 |
|
*Stock available in Belgium will be delivered in 1 to 3 days
*Stock available in Japan will be delivered in 1 to 2 weeks (excludes regulated items and dry ice shipments).
Product Number | B5400 |
Purity / Analysis Method | >98.0%(T) |
Molecular Formula / Molecular Weight | C__2__4H__1__6F__1__2N__4P__2Pd = 756.77 |
Physical State (20 deg.C) | Solid |
Storage Temperature | Room Temperature (Recommended in a cool and dark place, <15°C) |
Packaging and Container | 1G-Glass Bottle with Plastic Insert (View image), 200MG-Glass Bottle with Plastic Insert (View image) |
CAS RN | 113173-22-1 |
Reaxys Registry Number | 16958389 |
PubChem Substance ID | 354335751 |
Specifications
Appearance | Light yellow to Brown powder to crystal |
Purity(Chelometric Titration) | min. 98.0 % |
Properties (reference)
GHS
Pictogram | |
Signal Word | Warning |
Hazard Statements | H315 : Causes skin irritation. H319 : Causes serious eye irritation. |
Precautionary Statements | P264 : Wash skin thoroughly after handling. P280 : Wear protective gloves/ eye protection/ face protection. P302 + P352 : IF ON SKIN: Wash with plenty of water. P337 + P313 : If eye irritation persists: Get medical advice/ attention. P362 + P364 : Take off contaminated clothing and wash it before reuse. P332 + P313 : If skin irritation occurs: Get medical advice/ attention. |
Related Laws:
Transport Information:
HS Number | 2843909000 |
Application
Palladium Catalyst for the Synthesis of 2,4,5-Trisubstituted Imidazoles
Experimental procedure2): DMA (0.5 mol/L) is added to a vessel and degassed by a freeze-pump-thaw cycle (3 times). To this is added Pd(OAc)2 (5 mol%), tri(2-furyl)phosphine (10 mol%), K2CO3 (1 eq.), 1-methylimidazole (1 mmol), and 4-bromobenzotrifluoride (1 eq.). The mixture is stirred for 4 h at 150 °C under an argon atmosphere. The reaction mixture is then cooled to room temperature. To this is added iodobenzene (1 eq.), Cs2CO3 (1 eq.), and [Pd(phen)2](PF6)2 (5 mol%), and the mixture is stirred for 4 h at 150 °C under an argon atmosphere. Subsequently, 4-iodoanisole (3 eq.), Cs2CO3 (3 eq.), and [Pd(phen)2](PF6)2 (15 mol%) are split into 6 portions, respectively, and added portionwise to the reaction mixture every 0.5 h at 150 °C. The resulting mixture is stirred at that temperature for 20 h under an argon atmosphere. The reaction mixture is filtered through a Celite pad and concentrated in vacuo. The residue is purified by flash column chromatography on silica gel (hexane:EtOAc = 10:1) to give 1 in 37% yield (151 mg).
References
- 1)Direct Arylation of Simple Azoles Catalyzed by 1,10-Phenanthroline Containing Palladium Complexes: An Investigation of C4 Arylation of Azoles and the Synthesis of Triarylated Azoles by Sequential Arylation
- 2)One-pot Sequential Direct C-H Bond Arylation of Azoles Catalyzed by [Pd(phen)2](PF6)2: Synthetic Methods for Triarylated Azoles
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