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Merck
모든 사진(6)

주요 문서

222380

Sigma-Aldrich

Allylpalladium(II) chloride dimer

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98%

동의어(들):

Bis((η3-allyl)(chloro)palladium), Di-ο-allyldi-μ-chlorodipalladium, [PdCl(C3H5)]2

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About This Item

실험식(Hill 표기법):
C6H10Cl2Pd2
CAS Number:
Molecular Weight:
365.89
Beilstein:
4124623
EC Number:
MDL number:
UNSPSC 코드:
12161600
PubChem Substance ID:
NACRES:
NA.22

Quality Level

분석

98%

형태

solid

반응 적합성

core: palladium
reaction type: Cross Couplings
reagent type: catalyst
reaction type: C-H Activation

환경친화적 대안 제품 특성

Catalysis
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환경친화적 대안 카테고리

저장 온도

2-8°C

SMILES string

Cl[Pd]CC=C.Cl[Pd]CC=C

InChI

1S/2C3H5.2ClH.2Pd/c2*1-3-2;;;;/h2*3H,1-2H2;2*1H;;/q;;;;2*+1/p-2

InChI key

TWKVUTXHANJYGH-UHFFFAOYSA-L

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일반 설명

Allylpalladium(II) chloride dimer is employed as catalyst in Heck reaction. It also participates as catalyst in the tandem nucleophilic allylation-alkoxyallylation reaction of the alkynylaldehydes with allyl chloride and allyltributylstannane.
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애플리케이션

Allylpalladium(II) chloride dimer has been employed for the following studies:
  • Synthesis of cationic palladium cataysts, used in the microwave-assisted Heck arylation.
  • Synthesis of N-heterocyclic carbene-palladium-η3-allyl chloride complexes, which are efficient catalyst for the Suzuki-Miyaura cross-coupling of aryl bromides and activated aryl chlorides.
  • Synthesis of 1,4-diallyl-1,2-dihydroisoquinolines.
  • As catalyst for greener Buchwald-Hartwig coupling in TPGS-750-M.

On the Way Towards Greener Transition-Metal-Catalyzed Processes as Quantified by E Factors

픽토그램

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신호어

Warning

유해 및 위험 성명서

Hazard Classifications

Skin Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

개인 보호 장비

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


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문서 라이브러리 방문

European Journal of Organic Chemistry, 3122-3122 (2007)
Matthias Eckhardt et al.
Journal of the American Chemical Society, 125(45), 13642-13643 (2003-11-06)
A Pd/N-heterocyclic carbene-based catalyst achieves the Sonogashira coupling of an array of functionalized, beta-hydrogen-containing alkyl bromides and iodides under mild conditions. By furnishing the first example of a nonphosphine-based palladium catalyst for cross-coupling unactivated alkyl electrophiles, this study provides an
The Journal of Organic Chemistry, 59, 5034-5034 (1994)
Synthesis, 1683-1683 (2007)
Recyclable Palladium Catalysts for the Heck/Sonogashira Reaction under Microwave-assisted Thermomorphic Conditions.
Lu N, et al.
J. Chin. Chem. Soc. (2014)

문서

A variety of palladium-catalyzed cross-coupling reactions can be run under room temperature conditions in water with TPGS- 750-M, using a variety of commercially available palladium complexes and ligands.

프로토콜

TPGS-750-M surfactant enables various reactions in water at room temperature, enhancing efficiency and versatility in synthesis.

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