68630-80-8
di-mu-chlorodichlorobis[1,1'-thiobis[butane]]dipalladium
CAS: 68630-80-8
Molecular Formula: C16H36Cl4Pd2S2
68630-80-8 - Names and Identifiers
| Name | di-mu-chlorodichlorobis[1,1'-thiobis[butane]]dipalladium |
| Synonyms | di-mu-chlorodichlorobis[1,1'-thiobis[butane]]dipalladium |
| CAS | 68630-80-8 |
| EINECS | 271-918-9 |
68630-80-8 - Physico-chemical Properties
| Molecular Formula | C16H36Cl4Pd2S2 |
| Molar Mass | 647.23904 |
68630-80-8 - Introduction
di-mu-chlorodichlorobis[1,1 '-thiobis[butane]] dipallium is a metal-organic compound with the formula [Pd2Cl2(SC4H8) 2cl2]. It is a colorless crystal or yellow solid, insoluble in water, but readily soluble in organic solvents.
di-mu-chlorodichlorobis[1,1 '-thiobis[butane]]dipalladium can be used as a catalyst, especially in organic synthesis. It can catalyze coupling reactions of halogenated hydrocarbons, such as Suzuki coupling reaction and stile coupling reaction. These reactions have important applications in drug synthesis and materials chemistry.
The method of preparing di-mu-chlorodichlorobis[1,1 '-thiobis[butane]]dipalladium is relatively complicated, usually by mixing 1,1'-disulfide dioxide with hydrochloride to generate 1,1 '-dichlorodisulfide, and then reacted with sodium tetrachloride to form 1,1'-dichlorodisulfide sodium. Sodium 1,1 '-dichlorodisulfide is then reacted with palladium chloride to give 1,1'-dichlorodithiobiphenylochloride BIS [butane-1,4-disulfide] diaminodipalladium.
Regarding safety information, di-mu-chlorodichlorobis[1,1 '-thiobis[butane]]dipalladium needs to comply with relevant safety procedures when handling and storing. It is a toxic substance that may produce Irritating odors and vapors, avoid contact with skin and eyes. Wear appropriate personal protective equipment such as gloves, goggles and laboratory coats when handling. Avoid inhaling gas, dust or steam during use and handling, and ensure that the operating area is well ventilated.
di-mu-chlorodichlorobis[1,1 '-thiobis[butane]]dipalladium can be used as a catalyst, especially in organic synthesis. It can catalyze coupling reactions of halogenated hydrocarbons, such as Suzuki coupling reaction and stile coupling reaction. These reactions have important applications in drug synthesis and materials chemistry.
The method of preparing di-mu-chlorodichlorobis[1,1 '-thiobis[butane]]dipalladium is relatively complicated, usually by mixing 1,1'-disulfide dioxide with hydrochloride to generate 1,1 '-dichlorodisulfide, and then reacted with sodium tetrachloride to form 1,1'-dichlorodisulfide sodium. Sodium 1,1 '-dichlorodisulfide is then reacted with palladium chloride to give 1,1'-dichlorodithiobiphenylochloride BIS [butane-1,4-disulfide] diaminodipalladium.
Regarding safety information, di-mu-chlorodichlorobis[1,1 '-thiobis[butane]]dipalladium needs to comply with relevant safety procedures when handling and storing. It is a toxic substance that may produce Irritating odors and vapors, avoid contact with skin and eyes. Wear appropriate personal protective equipment such as gloves, goggles and laboratory coats when handling. Avoid inhaling gas, dust or steam during use and handling, and ensure that the operating area is well ventilated.
Last Update：2024-04-09 20:02:46
