![Paladyòm, [1,3-bis[2,6-bis (1-methylethyl)phenyl]-1,3-dihydro-2H-imidazol-2-iliden]chloro [(1,2,3-h)-(2E )-3-phenyl-2-propen-1-yl]-,stereoisomer Cas:884879-23-6 Imaj En](http://cdn.globalso.com/xdbiochems/884879-23-6.jpg)
Paladyòm, [1,3-bis[2,6-bis (1-methylethyl)phenyl]-1,3-dihydro-2H-imidazol-2-iliden]chloro [(1,2,3-h)-(2E )-3-phenyl-2-propen-1-yl]-, estereoizomer Cas:884879-23-6
| Nimewo Katalòg | XD90699 |
| Non pwodwi | Paladyòm, [1,3-bis[2,6-bis (1-methylethyl)phenyl]-1,3-dihydro-2H-imidazol-2-iliden]chloro [(1,2,3-h)-(2E )-3-phenyl-2-propen-1-yl]-,stereoizomer |
| CAS | 884879-23-6 |
| Fòmil molekilè | NeolystCX31 |
| Pwa molekilè | - |
| Detay Depo | Tanperati chanm |
Spesifikasyon pwodwi
| Esè | 99% |
| Pwen k ap fonn | 205-208 °C |
Yo rapòte itilizasyon dezyèm jenerasyon [(NHC) Pd (R-allyl) Cl] konplèks pou Suzuki-Miyaura ak Buchwald-Hartwig reyaksyon kwa-couplage ki enplike alogen eteroaromatik nan tanperati chanm.Egzanp yo premye nan tanperati chanm Suzuki-Miyaura kwa-kouplage nan klori aryl dezaktive ak asid alkenil boronik yo tou divilge.Ranplasman tèminal nan pati alyl konplèks paladyòm nan fasilite deklanchman li nan tanperati chanm ki mennen nan espès katalitik trè aktif ki pèmèt transfòmasyon katalitik prezan yo dwe fèt rapidman lè l sèvi avèk kondisyon reyaksyon trè modere.Chajman katalis yo ka ba 10 ppm pou aminasyon aryl Buchwald-Hartwig ak 50 ppm pou reyaksyon Suzuki-Miyaura.
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