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Merck
모든 사진(1)

주요 문서

924377

Sigma-Aldrich

Palladium(II) Acetate ChemBeads

동의어(들):

Acetic acid palladium salt, Bis(acetato)palladium, Diacetatopalladium, Diacetoxypalladium

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250 MG
₩98,049
1 G
₩251,314

₩98,049


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250 MG
₩98,049
1 G
₩251,314

About This Item

Linear Formula:
Pd(OCOCH3)2
CAS Number:
MDL number:
UNSPSC 코드:
12352302
NACRES:
NA.82
양식:
solid

₩98,049


구입 가능 여부는 고객센터에 문의하십시오.

벌크 견적 요청

양식

solid

Quality Level

구성

~ 4 wt.% loading of catalyst

반응 적합성

core: palladium
reaction type: Buchwald-Hartwig Cross Coupling Reaction

core: palladium
reaction type: Heck Reaction

core: palladium
reaction type: Hiyama Coupling

core: palladium
reaction type: Negishi Coupling

core: palladium
reaction type: Sonogashira Coupling

core: palladium
reaction type: Stille Coupling

core: palladium
reaction type: Suzuki-Miyaura Coupling

reaction type: Cross Couplings
reagent type: catalyst

SMILES string

[Pd](OC(=O)C)OC(=O)C

InChI

1S/2C2H4O2.Pd/c2*1-2(3)4;/h2*1H3,(H,3,4);/q;;+2/p-2

InChI key

YJVFFLUZDVXJQI-UHFFFAOYSA-L

일반 설명

Palladium(II) acetate is a homogenous oxidation catalyst. It participates in the activation of alkenic and aromatic compounds towards oxidative inter- and intramolecular nucleophilic reactions. Crystals of palladium(II) acetate have a trimeric structure, having symmetry D3h. Each of the palladium atoms in the crystals are joined to the other two by double acetate bridges. Microencapsulation of palladium(II) acetate in polyurea affords polyurea-encapsulated palladium(II) acetate. It is a versatile heterogeneous catalyst for various phosphine-free cross-coupling reactions. It participates as catalyst in the Heck coupling reaction of pthalides with different alkenes.

애플리케이션

Catalyst for an intramolecular coupling of aryl bromides with alcohols giving 1,3-oxazepines. Preparation of cyclic ureas via palladium-catalyzed intramolecular cyclization.

ChemBeads are chemical coated glass beads. ChemBeads offer improved flowability and chemical uniformity perfect for automated solid dispensing and high-throughput experimentation. The method of creating ChemBeads uses no other chemicals or surfactants allowing the user to accurately dispense sub-milligram amounts of chemical.

Learn more about ChemBeads products

For larger scale uses, product also available in powdered form (205869) & (520764)

픽토그램

CorrosionExclamation markEnvironment

신호어

Danger

유해 및 위험 성명서

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Skin Sens. 1A

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable


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문서 라이브러리에서 최근에 구매한 제품에 대한 문서를 찾아보세요.

문서 라이브러리 방문

Novel formation of 1,3-oxazepine heterocycles via palladium-catalyzed intramolecular coupling reaction.
Ma Chen, et al.
Tetrahedron, 62, 9002-9009 (2006)
The First Stereoselective Palladium-Catalyzed Cyclocarbonylation of β,γ-Substituted Allylic Alcohols.
Brunner M, et al.
The Journal of Organic Chemistry, 62, 7565-7568 (1997)
Palladium-catalyzed β-arylation of modified vinyl ethers with aryl triflates..
Badone D, et al.
Tetrahedron Letters, 34, 3603-3606 (1993)
Palladium-Catalyzed Amination of Aryl Triflates.
Wolfe J P, et al.
The Journal of Organic Chemistry, 62, 1264-1267 (1997)
Mark McLaughlin et al.
Organic letters, 8(15), 3311-3314 (2006-07-14)
[Structure: see text] An efficient regioselective method for the preparation of structurally diverse imidazopyridinones and benzoimidazolones starting from readily available and economical starting materials is described. High-yielding reductive alkylation of electron-deficient o-haloarylamines followed by treatment with inexpensive N-chlorosulfonyl isocyanate afforded

문서

ChemBeads, catalyst-coated glass beads, dispense solid chemical reagents for nanomole-scale high-throughput reaction screening.

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