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化驗
97%
形狀
solid
反應適用性
core: palladium
reaction type: Buchwald-Hartwig Cross Coupling Reaction
reaction type: Cross Couplings
reaction type: Heck Reaction
reaction type: Hiyama Coupling
reaction type: Negishi Coupling
reaction type: Sonogashira Coupling
reaction type: Stille Coupling
reaction type: Suzuki-Miyaura Coupling
reagent type: catalyst
mp
218-220 °C
儲存溫度
2-8°C
SMILES 字串
Cl[Pd].Cl[Pd].[CH2][CH][CH]c1ccccc1.[CH2][CH][CH]c2ccccc2
InChI
1S/2C9H9.2ClH.2Pd/c2*1-2-6-9-7-4-3-5-8-9;;;;/h2*2-8H,1H2;2*1H;;/q;;;;2*+1/p-2
InChI 密鑰
SHWAPUDBEQXXLQ-UHFFFAOYSA-L
應用
氯化钯(π-肉桂基)二聚体可在以下情形中用作催化剂:
也可在α酰胺不对称芳基化中用作钯来源。
- 氨交叉偶联反应,用于合成芳香胺。
- 芳基三氟甲基磺酸至氟化物转换。
也可在α酰胺不对称芳基化中用作钯来源。
儲存類別代碼
11 - Combustible Solids
水污染物質分類(WGK)
WGK 3
閃點(°F)
Not applicable
閃點(°C)
Not applicable
其他客户在看
Evidence for in situ catalyst modification during the Pd-catalyzed conversion of aryl triflates to aryl fluorides.
Journal of the American Chemical Society, 133(45), 18106-18109 (2011)
Matching the chirality of monodentate N-heterocyclic carbene ligands: a case study on well-defined palladium complexes for the asymmetric ?-arylation of amides.
Organic Letters, 10(24), 5569-5572 (2008)
AP, N?Ligand for Palladium?Catalyzed Ammonia Arylation: Coupling of Deactivated Aryl Chlorides, Chemoselective Arylations, and Room Temperature Reactions
Angewandte Chemie (International Edition in English), 122(24), 4165-4168 (2010)
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