[1,2-Bis(dicyclohexylphosphino)ethane]palladium(II) chloride
[1,2-Bis(dicyclohexylphosphino)ethane]palladium(II) chloride
CAS: 96165-44-5
Molecular Formula: C26H48Cl2P2Pd
[1,2-Bis(dicyclohexylphosphino)ethane]palladium(II) chloride - Names and Identifiers
[1,2-Bis(dicyclohexylphosphino)ethane]palladium(II) chloride - Physico-chemical Properties
| Molecular Formula | C26H48Cl2P2Pd |
| Molar Mass | 599.932842 |
| Melting Point | >300°C |
| Storage Condition | under inert gas (nitrogen or Argon) at 2-8°C |
[1,2-Bis(dicyclohexylphosphino)ethane]palladium(II) chloride - Risk and Safety
| Hazard Symbols | Xn - Harmful |
| Risk Codes | R22 - Harmful if swallowed R36/37/38 - Irritating to eyes, respiratory system and skin. R40 - Limited evidence of a carcinogenic effect R43 - May cause sensitization by skin contact |
| Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36/37 - Wear suitable protective clothing and gloves. |
| WGK Germany | 3 |
[1,2-Bis(dicyclohexylphosphino)ethane]palladium(II) chloride - Introduction
[1,2-Bis(dicyclohexylphosphino)ethane]palladium(II) chloride] is an organometallic compound. Its chemical formula is [PdCl2(dppc)], where dppc represents a [1,2-bis (dicyclohexyl) ethane] ligand.
In terms of properties,[1,2-Bis(dicyclohexylphosphino)ethane]palladium(II) chloride] is a colorless solid. It has good solubility at room temperature and is soluble in many organic solvents such as benzene and dimethylformamide. It is thermally stable and can maintain structural integrity at high temperatures.
[1,2-Bis(dicyclohexylphosphino)ethane]palladium(II) chloride] is widely used as a catalyst in organic synthesis reactions. It is often used as a catalyst for oxidation, reduction, carbonylation and coupling reactions. The compound plays an important role in many important organic synthesis reactions, such as Suzuki coupling, Stille coupling and Heck reaction. The catalysts for these reactions usually employ [1,2-Bis(dicyclohexylphosphino)ethane]palladium(II) chloride] complexes.
Preparatively,[1,2-Bis(dicyclohexylphosphino)ethane]palladium(II) chloride] can be obtained by reacting a vinylphenyldiphosphine ligand (dppc) with palladium(II) chloride. This compound can be prepared by heating a mixture of the diphosphine ligand and palladium (II) chloride under appropriate conditions.
In terms of safety information,[1,2-Bis(dicyclohexylphosphino)ethane]palladium(II) chloride] generally has low toxicity under normal experimental conditions, but it is still an organometallic compound and needs to be handled according to laboratory safety procedures. When using, observe relevant safety procedures, such as wearing gloves and goggles to avoid contact with or inhalation of the compound. In addition, it should be stored in a sealed container, away from fire and oxidizing agents, to prevent its decomposition or deterioration.
In terms of properties,[1,2-Bis(dicyclohexylphosphino)ethane]palladium(II) chloride] is a colorless solid. It has good solubility at room temperature and is soluble in many organic solvents such as benzene and dimethylformamide. It is thermally stable and can maintain structural integrity at high temperatures.
[1,2-Bis(dicyclohexylphosphino)ethane]palladium(II) chloride] is widely used as a catalyst in organic synthesis reactions. It is often used as a catalyst for oxidation, reduction, carbonylation and coupling reactions. The compound plays an important role in many important organic synthesis reactions, such as Suzuki coupling, Stille coupling and Heck reaction. The catalysts for these reactions usually employ [1,2-Bis(dicyclohexylphosphino)ethane]palladium(II) chloride] complexes.
Preparatively,[1,2-Bis(dicyclohexylphosphino)ethane]palladium(II) chloride] can be obtained by reacting a vinylphenyldiphosphine ligand (dppc) with palladium(II) chloride. This compound can be prepared by heating a mixture of the diphosphine ligand and palladium (II) chloride under appropriate conditions.
In terms of safety information,[1,2-Bis(dicyclohexylphosphino)ethane]palladium(II) chloride] generally has low toxicity under normal experimental conditions, but it is still an organometallic compound and needs to be handled according to laboratory safety procedures. When using, observe relevant safety procedures, such as wearing gloves and goggles to avoid contact with or inhalation of the compound. In addition, it should be stored in a sealed container, away from fire and oxidizing agents, to prevent its decomposition or deterioration.
Last Update：2024-04-10 22:30:50
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