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XPHOS PD G3, 95%
Кат. №: 763381-1G
Производитель: Sigma-Aldrich
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XPHOS PD G3, 95%
Main image
Кат. №: 763381-1G
Производитель: Sigma-Aldrich
Кол-во:
Цена по запросу
Товар оформляется под заказ
Main image
Печать
XPHOS PD G3, 95%
Кат. №: 763381-1G
Производитель: Sigma-Aldrich
Кол-во:
Цена по запросу
Товар оформляется под заказ
Description General description XPhos Pd G3 is a third generation (G3) Buchwald precatalyst. It is air, moisture and thermally-stable and is highly soluble in a wide range of common organic solvents. It has long life in solutions. XPhos Pd G3 is an excellent reagent for Suzuki cross-coupling reactions. Some of its unique features include lower catalyst loadings, shorter reaction time, efficient formation of the active catalytic species and accurate control of ligand: palladium ratio. Application XPhos Pd G3 may be used in the following reactions: • Cyanation reaction of heterocyclic halides. • Coupling of heteroaryl chlorides with polyfluoroaryl zinc reagents. • Coupling of 2,6-difluorophenylboronic acid with (hetero)aryl chlorides. Packaging 1, 5 g in glass bottle 250 mg in glass bottle
Related Categories
Buchwald 3rd Generation Palladacycles, Buchwald Ligands and Complexes, Catalysis and Inorganic Chemistry, Chemical Synthesis, Cross-Coupling, Homogeneous Pd Catalysts, Palladium Catalysts More... Quality Level
Дорогой клиент, на сайте внедрена нейросеть для сбора информации о товаре. Это может привести к незначительным расхождениям в характеристиках продукции.
Description General description XPhos Pd G3 is a third generation (G3) Buchwald precatalyst. It is air, moisture and thermally-stable and is highly soluble in a wide range of common organic solvents. It has long life in solutions. XPhos Pd G3 is an excellent reagent for Suzuki cross-coupling reactions. Some of its unique features include lower catalyst loadings, shorter reaction time, efficient formation of the active catalytic species and accurate control of ligand: palladium ratio. Application XPhos Pd G3 may be used in the following reactions: • Cyanation reaction of heterocyclic halides. • Coupling of heteroaryl chlorides with polyfluoroaryl zinc reagents. • Coupling of 2,6-difluorophenylboronic acid with (hetero)aryl chlorides. Packaging 1, 5 g in glass bottle 250 mg in glass bottle
Related Categories
Buchwald 3rd Generation Palladacycles, Buchwald Ligands and Complexes, Catalysis and Inorganic Chemistry, Chemical Synthesis, Cross-Coupling, Homogeneous Pd Catalysts, Palladium Catalysts More... Quality Level
Дорогой клиент, на сайте внедрена нейросеть для сбора информации о товаре. Это может привести к незначительным расхождениям в характеристиках продукции.