Name | dichloro[(1,2,5,6-η)-cycloocta-1,5-diene]palladium |
Synonyms | dichloropalladium (1Z,5Z)-cycloocta-1,5-diene Allylpalladium chloride dimer Dichloro(1,5-cyclooctadiene)palladium(II) DICHLORO(1,5-CYCLOOCTADIENE)PALLADIUM(II) (1,5-CYCLOOCTADIENE)PALLADIUM(II)CHLORIDE DICHLORO(CYCLOOCTA-1,5-DIENE)PALLADIUM(II) 1,5-CYCLOOCTADIENEPALLADIUM(II) DICHLORIDE 1,5-Cyclooctadienepalladium(II) Dichloride DICHLORO(1,5-CYCLOOCTYLDIENE)PALLADIUM(II) DICHLORO(CYCLOOCTA-1,5-DIENE)PALLADATE (II) DICHLORO(ETA-CYCLOOCTA-1,5-DIENE)PALLADIUM (II) dichloro[(1,2,5,6-η)-cycloocta-1,5-diene]palladium dichloro[(1,2,5,6-eta)-1,5-cyclooctadiene]-palladiu |
CAS | 12107-56-1 |
EINECS | 235-161-8 |
InChI | InChI=1/C8H12.2ClH.Pd/c1-2-4-6-8-7-5-3-1;;;/h1-2,7-8H,3-6H2;2*1H;/q;;;+2/p-2/b2-1-,8-7-;; |
InChIKey | NEKYMUKEOUDFPP-XRGHXPOKSA-L |
Molecular Formula | C8H12Cl2Pd |
Molar Mass | 285.51 |
Melting Point | 210 °C (dec.) (lit.) |
Boling Point | 153.5°C at 760 mmHg |
Flash Point | 31.7°C |
Water Solubility | insoluble |
Solubility | Soluble in dichloromethane |
Vapor Presure | 4.25mmHg at 25°C |
Appearance | Yellow crystal |
Color | yellow |
Storage Condition | Inert atmosphere,Room Temperature |
Sensitive | Hygroscopic |
MDL | MFCD00012412 |
Use | Catalyst C- C and C- N bond formation for Heck coupling reaction of alkynes with alkenes, Suzuki coupling reaction of aryl bromide, allyl substitution reaction of oxime with allyl ester, and methoxycarbonyl reaction of iodobenzene. |
Hazard Symbols | Xi - Irritant |
Risk Codes | 36/37/38 - Irritating to eyes, respiratory system and skin. |
Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S37/39 - Wear suitable gloves and eye/face protection |
WGK Germany | 3 |
TSCA | Yes |
HS Code | 28439000 |
EPA chemical information | Information provided by: ofmpub.epa.gov (external link) |
Use | The formation of C- C bonds and C- N bonds of the catalyst, used for the Heck coupling reaction of alkynes and alkenes, the Suzuki coupling reaction of aryl bromide, the allyl substitution reaction of oxime and allyl ester, and the methoxycarbonyl reaction of iodobenzene. |