Dichloro[9,9-dimethyl-4,5-bis(diphenylphosphino)xanthene]palladium(II) structure 
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        Common Name | Dichloro[9,9-dimethyl-4,5-bis(diphenylphosphino)xanthene]palladium(II) | ||
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| CAS Number | 205319-10-4 | Molecular Weight | 755.94 | |
| Density | N/A | Boiling Point | N/A | |
| Molecular Formula | C39H32Cl2OP2Pd | Melting Point | 287 °C(dec.) | |
| MSDS | USA | Flash Point | N/A | |
            Use of Dichloro[9,9-dimethyl-4,5-bis(diphenylphosphino)xanthene]palladium(II)Pd(Xantphos)Cl2 is a biochemical reagent that can be used as a biological material or organic compound for life science related research.  | 
    
| Name | dichloropalladium,(5-diphenylphosphanyl-9,9-dimethylxanthen-4-yl)-diphenylphosphane | 
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| Synonym | More Synonyms | 
| Description | Pd(Xantphos)Cl2 is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | 
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| Related Catalog | 
| Melting Point | 287 °C(dec.) | 
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| Molecular Formula | C39H32Cl2OP2Pd | 
| Molecular Weight | 755.94 | 
| Exact Mass | 754.033997 | 
| PSA | 36.41000 | 
| LogP | 1.64260 | 
| RIDADR | NONH for all modes of transport | 
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                                         ~82%  
                                            Dichloro[9,9-di... CAS#:205319-10-4  | 
                                
| Literature: European Journal of Inorganic Chemistry, , # 2 p. 155 - 157 | 
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| DownStream 0 | |
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                                    Palladium-catalyzed esterification of aryl halides using aryl formates without the use of external carbon monoxide.
                                    
                                    
                                     Chem. Commun. (Camb.) 48 , 8012, (2012) Aryl formates are efficient carbon monoxide sources in palladium-catalyzed esterification of aryl halides. The carbonylation readily proceeds at ambient pressure without the use of external carbon mon...  | 
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                                    Palladium-catalyzed oxidative carbonylation of benzylic C-H bonds via nondirected C(sp3)-H activation.
                                    
                                    
                                     J. Am. Chem. Soc. 134 , 9902, (2012) A new strategy for generating benzylpalladium reactive species from toluenes via nondirected C(sp(3))-H activation has been developed. This led to construction of an efficient Pd-catalyzed reaction pr...  | 
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                                    Improved carbonylation of heterocyclic chlorides and electronically challenging aryl bromides.
                                    
                                    
                                     Org. Lett. 6 , 2097, (2004) [reaction: see text] Optimized conditions are described that effect the carbonylation of diverse heterocyclic chlorides to yield the desired alkyl esters. In addition, bromoanilines and bromoanisoles,...  | 
                                
| Palladium(2+) chloride - (9,9-dimethyl-9H-xanthene-4,5-diyl)bis(diphenylphosphine) (1:2:1) | 
| [4,5-Bis(diphenylphosphino)-9,9-dimethylxanthene]dichloropalladium(II) | 
| Phosphine, 1,1'-(9,9-dimethyl-9H-xanthene-4,5-diyl)bis[1,1-diphenyl-, palladium(2+) salt, hydrochloride (1:1:2) | 
| [4,5-Bis(diphenylphosphino)-9,9-dimethylxanthene]palladium(II) Dichloride | 
| Dichloro[9,9-dimethyl-4,5-bis(diphenylphosphino)xanthene]palladium(II) |