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CAS RN: 1375325-71-5 | Product Number: C2734
Chloro[(tri-tert-butylphosphine)-2-(2-aminobiphenyl)]palladium(II)
![Chloro[(tri-tert-butylphosphine)-2-(2-aminobiphenyl)]palladium(II) No-Image](/medias/C2734.jpg?context=bWFzdGVyfHJvb3R8NjQ5NTl8aW1hZ2UvanBlZ3xhR1ZpTDJnMU1DODRPVEl3TnpZd09EUTBNekU0TDBNeU56TTBMbXB3Wnd8MDE5Nzg4OWYwMDdiNmRmNGFiMDQ4NWRkMWI1MmIxYjAyODgzZGVhZDU0MWVlYjUwMzk1N2QxNDk5MGU1Y2QzOA)
Purity: >98.0%(T)
Synonyms:
Product Documents:
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Product Number | C2734 |
Purity / Analysis Method | >98.0%(T) |
Molecular Formula / Molecular Weight | C__2__4H__3__7ClNPPd = 512.41 |
Physical State (20 deg.C) | Solid |
Storage Temperature | Room Temperature (Recommended in a cool and dark place, <15°C) |
Store Under Inert Gas | Store under inert gas |
Condition to Avoid | Moisture Sensitive |
Packaging and Container | 1G-Glass Bottle with Plastic Insert (View image) |
CAS RN | 1375325-71-5 |
Reaxys Registry Number | 22750896 |
PubChem Substance ID | 253659744 |
MDL Number | MFCD21608496 |
Specifications
Appearance | Light yellow to Amber to Dark green powder to crystal |
Purity(Chelometric Titration) | min. 98.0 % |
Properties (reference)
Melting Point | 159 °C(dec.) |
GHS
Pictogram |
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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. P305 + P351 + P338 : IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. 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:
H.S.code* | 2843.90-000 |
Application
Palladium Complex Catalyzing Cross Coupling Reactions with Activating C-H Bond of Polyfluoroarenes
Experimental procedure: In a glovebox, to a vial containing bromobenzene (62 mg, 0.4 mmol), 1 (10.0 mg, 0.02 mmol), pivalic acid (20 mg, 0.2 mmol), K3PO4 (168 mg, 0.8 mmol) and DMA (1 mL) is added pentafluorobenzene (98 mg, 0.6 mmol). After stirring at 80 °C for 2-4 h, the reaction is quenched by the addition of NH4Cl solution. The product is extracted with ethyl acetate (3 x 15 mL) and the combined organic layer is washed with brine and dried with Na2SO4. After removal of solvents under vacuum, the crude product is purified by column chromatography (silica gel; hexanes) to give the corresponding product as a colorless oil (86% yield).
References
- tBu3P-Coordinated 2-Phenylaniline-Based Palladacycle Complexes as Precatalyst for Pd-Catalyzed Coupling Reactions of Aryl Halides with Polyfluoroarenes by a C–H Activation Strategy
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