推荐产品
形狀
solid
反應適用性
core: palladium
reaction type: Buchwald-Hartwig Cross Coupling Reaction
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
濃度
60% Pd
mp
678-680 °C (lit.)
密度
4 g/mL at 25 °C (lit.)
SMILES 字串
Cl[Pd]Cl
InChI
1S/2ClH.Pd/h2*1H;/q;;+2/p-2
InChI 密鑰
PIBWKRNGBLPSSY-UHFFFAOYSA-L
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相关类别
應用
氯化钯(II)可用于催化以下反应:
- 在改良Sonogashira-Cassar-Heck条件下,末端炔烃与芳基碘化物或溴化物之间的交叉偶联反应。
- 有机碲与一氧化碳的羰基化反应,形成相应的甲基羧酸酯。
- 烯丙基酯在乙酸中的异构化反应。
- 胺的酰化反应,形成异氰酸酯。
其他說明
综述
訊號詞
Danger
危險分類
Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Met. Corr. 1 - Skin Sens. 1
儲存類別代碼
8B - Non-combustible corrosive hazardous materials
水污染物質分類(WGK)
WGK 3
閃點(°F)
Not applicable
閃點(°C)
Not applicable
個人防護裝備
Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
其他客户在看
Carbonylation of Amines in the Presence of Palladium (II) Chloride. A New Route to Isocyanates.
The Journal of Organic Chemistry, 31(2), 596-597 (1966)
Palladium (II)-catalyzed exchange and isomerization reactions. III. Allylic esters isomerization in acetic acid catalyzed by palladium (II) chloride.
Journal of the American Chemical Society, 94(15), 5200-5206 (1972)
Palladium (II) Chloride and a (Dipyridin?2?ylmethyl) amine?Derived Palladium (II) Chloride Complex as Highly Efficient Catalysts for the Synthesis of Alkynes in Water or in NMP and of Diynes in the Absence of Reoxidant.
European Journal of Organic Chemistry, 2005(19), 4073-4081 (2005)
Accounts of Chemical Research, 12, 146-146 (1979)
Palladium (II) chloride catalyzed carbonylation of organic tellurides with carbon monoxide.
The Journal of Organic Chemistry, 52(22), 4859-4863 (1987)
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