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741248

Sigma-Aldrich

双三苯基膦二氯化钯

同義詞:

PdCl2(PPh3)2, 三苯基膦氯化钯, 二氯二(三苯基膦)钯(II)

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About This Item

線性公式:
[(C6H5)3P]2PdCl2
CAS號碼:
13965-03-2
分子量：:
701.90
Beilstein:
4935975
EC號碼:
237-744-2
MDL號碼:
MFCD00009593
分類程式碼代碼:
12161600
PubChem物質ID:
329765477
NACRES:
NA.22

形狀

solid

品質等級

100

反應適用性

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
core: palladium
reagent type: ligand

官能基

phosphine

SMILES 字串

Cl[Pd]Cl.c1(P(c2ccccc2)c3ccccc3)ccccc1.c4(P(c5ccccc5)c6ccccc6)ccccc4

InChI

1S/2C18H15P.2ClH.Pd/c2*1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18;;;/h2*1-15H;2*1H;/q;;;;+2/p-2

InChI 密鑰

YNHIGQDRGKUECZ-UHFFFAOYSA-L

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相關類別

應用

钯催化交叉偶联反应应用指南
二（三苯基膦）二氯化钯 (II) 通常用作通过 斯蒂尔偶联合成共轭聚合物的催化剂 。它也适用于其他偶联反应，如铃木 和 Sonogashira-偶联反应

相關產品

產品號碼
描述
訂價

象形圖

Exclamation mark
GHS07

訊號詞

Warning

危險聲明

H317,H413

危險分類

Aquatic Chronic 4 - Skin Sens. 1A

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

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分析證明 (COA)

Lot/Batch Number
MKCP4921
MKCL0869
MKCH6889
MKCH3689
MKCG2324

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Synthesis of quaternized zinc (II) and cobalt (II) phthalocyanines bearing pyridine-2-yl-ethynyl groups and their DNA binding properties.
Alishah MM, et al.
Turkish Journal of Chemistry, 42(2), 572-585 (2018)
Influence of catalytic systems in Stille polymerization on the electrochromic performance of diketopyrrolopyrrole-based conjugated polymers.
Neo WT, et al.
Materials Chemistry Frontiers. (2018)
New oligomeric poly (ether-imide) s containing diphenylsilane and dibenzofuran moieties. Synthesis and characterization.
Tundidor-Camba A, et al.
Journal of Macromolecular Science, Part A: Pure and Applied Chemistry, 55(4), 324-331 (2018)
Ganesan Bharathiraja et al.
Organic & biomolecular chemistry, 13(9), 2786-2792 (2015-01-22)
Various tetrasubstituted pyrroles/pyrazoles have been prepared from nitro-substituted 1,3-enynes with aromatic amines/hydrazines via a copper-catalyzed cascade aza-Michael addition, cyclization and aromatization at room temperature. This protocol is also effective for the synthesis of tetrasubstituted pyrazoles in high yields.
Hiroaki Imoto et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 21(34), 12105-12111 (2015-07-17)
Aggregation-induced emission (AIE)-active maleimide dyes, namely, 2-p-toluidino-N-p-tolylmaleimide, 3-phenyl-2-toluidino-N-p-tolylmaleimide, 2-p-thiocresyl-3-p-toluidino-N-p-tolylmaleimide, and 2,3-dithiocresyl-N-arylmaleimides, were synthesized by facile synthetic procedures. The dyes show intense emission in the solid state, and emission colors were controlled from green (λmax =527 nm) to orange (λmax =609 nm) by

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