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CAS RN: 1251667-99-8 | Product Number: C3456
(p-Cymene)bis(mesitylcarboxylato)ruthenium(II)
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Purity:
Synonyms:
- Ru(MesCO2)2(p-cymene)
- (p-Cymene)bis(2,4,6-trimethylbenzoato)ruthenium(II)
Product Documents:
| Size | Unit Price | Hyderabad | Japan* | Quantity |
|---|---|---|---|---|
| 500MG |
₹13,360.00
|
5 | 17 |
|
*Upon orders receipt, Hyderabad stocks will be dispatched on the same day.
*Items available in Japan warehouse will be dispatched in 10-12 working days.
*INR price is exclusive of domestic taxes applicable.
*TCI frequently reviews storage conditions to optimize them. Please note that the latest information on the storage temperature for the products is described on our website.
| Product Number | C3456 |
| Molecular Formula / Molecular Weight | C__3__0H__3__6O__4Ru = 561.68 |
| Physical State (20 deg.C) | Solid |
| Storage Temperature | Room Temperature (Recommended in a cool and dark place, <15°C) |
| Packaging and Container | 500MG-Glass Bottle with Plastic Insert (View image) |
| CAS RN | 1251667-99-8 |
| Reaxys Registry Number | 20874878 |
| PubChem Substance ID | 354335673 |
Specifications
| Appearance | Light yellow to Yellow to Orange powder to crystal |
| Elemental analysis(Carbon) | 61.00 to 67.00 % |
| NMR | confirm to structure |
Properties (reference)
GHS
Related Laws:
Transport Information:
Application
Ruthenium Catalyst for the meta-Selective Substitution Reaction
Experimental procedure1):
A mixture of [Ru(MesCO2)2(p-cymene)] (15.0 mg, 0.027 mmol), K2CO3 (1.04 mmol, 2.0 eq.), 2 (96.2 mg, 0.52 mmol) and 3 (282 mg, 1.43 mmol) in dioxane (2 mL) is stirred under N2 for 20 h at 100 °C. EtOAc (50 mL) and H2O (50 mL) are added to the reaction mixture at ambient temperature. The separated aqueous phase is extracted with EtOAc (2 × 50 mL). The combined organic layers are washed with brine (50 mL), dried over Na2SO4 and concentrated in vacuo. The residue is purified by silica gel column chromatography (hexane:EtOAc = 9:1) to yield 4 (108 mg, 71%) as a colorless oil.
A mixture of [Ru(MesCO2)2(p-cymene)] (15.0 mg, 0.027 mmol), K2CO3 (1.04 mmol, 2.0 eq.), 2 (96.2 mg, 0.52 mmol) and 3 (282 mg, 1.43 mmol) in dioxane (2 mL) is stirred under N2 for 20 h at 100 °C. EtOAc (50 mL) and H2O (50 mL) are added to the reaction mixture at ambient temperature. The separated aqueous phase is extracted with EtOAc (2 × 50 mL). The combined organic layers are washed with brine (50 mL), dried over Na2SO4 and concentrated in vacuo. The residue is purified by silica gel column chromatography (hexane:EtOAc = 9:1) to yield 4 (108 mg, 71%) as a colorless oil.
References
- 1)meta-Selective C-H Bond Alkylation with Secondary Alkyl Halides
- 2)Ruthenium(II)-Catalyzed Decarboxylative C-H Activation: Versatile Routes to meta-Alkenylated Arenes
- 3)C(sp3)-H Bond Arylations Catalyzed by Well-Defined [Ru(O2CMes)2(p-cymene)]
PubMed Literature
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