dichloro[(1,2,5,6-η)-cycloocta-1,5-diene]palladium CAS:12107-56-1
Hoc compositum late in synthesi organica adhibetur, praesertim in reactionibus copulationis transversalis palladio-catalysatis, ut reactio Heck, copulatio Suzuki-Miyaura, et reactio Stille. Hae reactiones essentiales sunt in formatione vinculorum carbonii-carbonii et carbonii-heteroatomi, permittentes constructionem efficientem molecularum organicarum complexarum. Dichloro[(1,2,5,6-η)-cycloocta-1,5-diene]palladium etiam in praeparatione pharmaceuticorum, agrochemicorum, et chemicorum subtilium adhibetur. Eius reactivitas et selectivitas id instrumentum pretiosum faciunt ad synthesim intermediorum clavium et ingredientium pharmaceuticorum activorum. Praeterea, hoc compositum in scientia materialium ad constructionem materiarum functionalium, inter quas polymera coordinationis et structurae metallo-organicae, adhibetur. Eius proprietates catalyticae conferunt ad evolutionem materiarum cum proprietatibus accommodatis ad usus in catalysi, conservatione gasorum, et sensu.
| Compositio | C8H12Cl2Pd |
| Examen | 99% |
| Aspectus | Vis alba |
| Numerus CAS | 12107-56-1 |
| Sarcinatio | Parvus et moles |
| Tempus Vitae | Biennium |
| Depositorium | In loco frigido et sicco servandum |
| Certificatio | ISO. |

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