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The chemical compound [Ru(OC(O)C2H5)2(CO)2(P(C6H5)3)2] is a complex organometallic compound containing ruthenium (Ru) as the central metal atom. It features two ethyl acetate ligands (OC(O)C2H5), two carbonyl ligands (CO), and two triphenylphosphine ligands (P(C6H5)3). [Ru(OC(O)C2H5)2(CO)2(P(C6H5)3)2] is characterized by its octahedral geometry, with the ruthenium atom coordinated to six ligands. It is known for its stability and is often used in catalytic applications, particularly in homogeneous catalysis due to its ability to activate small molecules like hydrogen and carbon monoxide. The presence of phosphine ligands contributes to the compound's electronic properties and steric environment, which can influence its reactivity and selectivity in various chemical transformations.

31267-50-2

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31267-50-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 31267-50-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,2,6 and 7 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 31267-50:
(7*3)+(6*1)+(5*2)+(4*6)+(3*7)+(2*5)+(1*0)=92
92 % 10 = 2
So 31267-50-2 is a valid CAS Registry Number.

31267-50-2Upstream product

31267-50-2Downstream Products

31267-50-2Relevant academic research and scientific papers

Synthesis and molecular structure of [RuCl{C(=CHPh)OC(=O)CH2CH3}(CO)(PPh3) 2]: A real intermediate in ruthenium complex-catalyzed selective synthesis of a (Z)-enol ester

Kawano, Hiroyuki,Masaki, Yoshiko,Matsunaga, Takahiro,Hiraki, Katsuma,Onishi, Masayoshi,Tsubomura, Taro

, p. 69 - 77 (2007/10/03)

Reaction of [RuCl(η2-O2CCH2CH3)(CO)(PPh 3)2] (1) and phenylacetylene gives [RuCl{C(=CHPh)OC(=O)CH2CH3}(CO)(PPh3) 2] (2a). The X-ray structure analysis of 2a reveals that it includes a (Z)-enol ester-like 1-propanoyloxy-2-phenylethenyl-C1,O ligand. In the catalytic addition of propanoic acid to phenylacetylene, the complex 2a acts as a real intermediate that gives (Z)-2-phenylethenyl propanoate, selectively. The presence of the free PPh3 in the reaction mixture depresses formation of some dicarbonylruthenium species that catalytically produce (E)- and Markovnikov-type enol esters.

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