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Merck
모든 사진(3)

문서

343706

Sigma-Aldrich

Dichloro(p-cymene)ruthenium(II) dimer

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동의어(들):

(p-Cymene)ruthenium(II) chloride dimer, Benzene, 1-methyl-4-(1-methylethyl)-, ruthenium complex

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모든 사진(3)

About This Item

Linear Formula:
[Ru(p-cymene)Cl2]2
CAS Number:
52462-29-0
Molecular Weight:
612.39
MDL number:
MFCD00064793
UNSPSC 코드:
12161600
PubChem Substance ID:
24861190
NACRES:
NA.22

반응 적합성

core: ruthenium
reagent type: catalyst
reaction type: C-H Activation

환경친화적 대안 제품 특성

Catalysis
Learn more about the Principles of Green Chemistry.

sustainability

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mp

247.0-250.0 °C (dec.) (lit.)

환경친화적 대안 카테고리

, Aligned

SMILES string

Cl[Ru]Cl.Cl[Ru]Cl.CC(C)c1ccc(C)cc1.CC(C)c2ccc(C)cc2

InChI

1S/2C10H14.4ClH.2Ru/c2*1-8(2)10-6-4-9(3)5-7-10;;;;;;/h2*4-8H,1-3H3;4*1H;;/q;;;;;;2*+2/p-4

InChI key

LAXRNWSASWOFOT-UHFFFAOYSA-J

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관련 카테고리

일반 설명

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Dichloro(p-cymene)ruthenium(II) dimer is a saturated 18-electron complex used as a starting material for the synthesis of organometallic complexes.

애플리케이션

Hydrosilylation Catalysts
Catalyst for greener amine synthesis by reduction of imines with PMHS or hydrogen-borrowing.

A Practical and Benign Synthesis of Primary Amines through Ruthenium-Catalyzed Reduction of Nitriles

Ruthenium-Catalyzed N-Alkylation of Amines and Sulfonamides Using Borrowing Hydrogen Methodology
Cyclometalated ruthenium complexes with arylimines and nitrogen-containing heterocycles via C-H bond activation

픽토그램

Exclamation mark
GHS07

신호어

Warning

유해 및 위험 성명서

H319

Hazard Classifications

Eye Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

시험 성적서(COA)

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문서 라이브러리 방문

One-step synthesis of low molecular weight poly (p-phenyleneethynylenevinylene) s via polyaddition of aromatic diynes by catalysis of the [Ru (p-cymene) Cl2] 2/AcOH system
Chiara P et al.
The Journal of Organic Chemistry, 73, 3892-3899 (2008)
Carina Sollert et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 21(14), 5380-5386 (2015-02-18)
The Ru-catalysed C2-H arylation of indoles and pyrroles by using boronic acids under oxidative conditions is reported. This reaction can be applied to tryptophan derivatives and tolerates a wide range of functional groups on both coupling partners, including bromides and
Bin Li et al.
Dalton transactions (Cambridge, England : 2003), 41(36), 10934-10937 (2012-08-15)
The reaction of [RuCl(2)(p-cymene)](2) with arylimines and 4 equiv. of KOAc in methanol at room temperature produces stable (N^C)-cyclometallated ruthenium(II) complexes via C-H bond activation/deprotonation. This method can be applied also to nitrogen-containing molecules: N-phenylpyrazole, 2-phenyl-2-oxazoline and benzo[h]quinoline. N-Phenyl-pyrazole, [RuCl(2)(p-cymene)](2)

문서

Hydrosilylation Catalyst

Trost group's protocol yields α-vinylsilanes from terminal acetylenes using [Cp*Ru(MeCN)3]PF6 catalyst and others for hydrosilylation.

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