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For more information, please refer to the Product Dating Information document: https://www.sigmaaldrich.com/deepweb/assets/sigmaaldrich/marketing/global/documents/449/386/product-dating-information-mk.pdf
8.14761
Tetrakis(triphenylphosphine)-palladium(0)
for synthesis
Sinónimos:
Tetrakis(triphenylphosphine)-palladium(0)
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About This Item
Nivel de calidad
Formulario
powder
idoneidad de la reacción
reagent type: catalyst
reaction type: Cross Couplings
mp
103-107 °C
temp. de almacenamiento
2-8°C
cadena SMILES
[Pd]([P](c%12ccccc%12)(c%11ccccc%11)c%10ccccc%10)([P](c9ccccc9)(c8ccccc8)c7ccccc7)([P](c6ccccc6)(c5ccccc5)c4ccccc4)[P](c3ccccc3)(c2ccccc2)c1ccccc1
InChI
1S/4C18H15P.Pd/c4*1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18;/h4*1-15H;
Clave InChI
NFHFRUOZVGFOOS-UHFFFAOYSA-N
Descripción general
Aplicación
- Preparation of tricationic tris(pyridylpalladium(II)) metallacyclophane as an anion receptor.: This research explores the synthesis of a tricationic tris(pyridylpalladium(II)) metallacyclophane, showcasing its potential as an anion receptor. The study emphasizes the versatility of palladium complexes in developing new molecular structures for various applications (Danjo et al., 2022).
- A Ligand-Enabled Palladium-Catalyzed Highly para-Selective Difluoromethylation of Aromatic Ketones.: This study demonstrates the use of a palladium catalyst for highly selective difluoromethylation of aromatic ketones, highlighting the catalyst′s efficiency in organic synthesis and its potential for developing pharmaceuticals (Tu et al., 2018).
- Viable pathways for the oxidative addition of iodobenzene to palladium(0)-triphenylphosphine-carbonyl complexes: a theoretical study.: This theoretical investigation explores the oxidative addition mechanisms of iodobenzene to palladium(0)-triphenylphosphine-carbonyl complexes, providing insights into the reactivity and applications of palladium catalysts in organic synthesis (Pálinkás et al., 2017).
- Morita-Baylis-Hillman Reaction of α,β-Unsaturated Ketones with Allylic Acetates by the Combination of Transition-Metal Catalysis and Organomediation.: The paper discusses a novel Morita-Baylis-Hillman reaction facilitated by palladium(0) catalysts, demonstrating its utility in constructing complex molecular architectures for pharmaceutical synthesis (Li et al., 2016).
- Synthesis of a sterically crowded atropisomeric 1,8-diacridylnaphthalene for dual-mode enantioselective fluorosensing.: This research highlights the synthesis of a novel atropisomeric compound using palladium(0) catalysts, focusing on its application in enantioselective fluorosensing, crucial for biochemical analyses (Mei et al., 2006).
Nota de análisis
Palabra de señalización
Warning
Frases de peligro
Consejos de prudencia
Clasificaciones de peligro
Acute Tox. 4 Oral
Código de clase de almacenamiento
11 - Combustible Solids
Clase de riesgo para el agua (WGK)
WGK 3
Punto de inflamabilidad (°F)
Not applicable
Punto de inflamabilidad (°C)
Not applicable
Certificados de análisis (COA)
Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»
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Products may be shipped at a different temperature than the recommended long-term storage temperature. If the product quality is sensitive to short-term exposure to conditions other than the recommended long-term storage, it will be shipped on wet or dry-ice. If the product quality is NOT affected by short-term exposure to conditions other than the recommended long-term storage, it will be shipped at ambient temperature. As shipping routes are configured for minimum transit times, shipping at ambient temperature helps control shipping costs for our customers. For more information, please refer to the Storage and Transport Conditions document: https://www.sigmaaldrich.com/deepweb/assets/sigmaaldrich/marketing/global/documents/316/622/storage-transport-conditions-mk.pdf
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