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32993-05-8

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  • High efficiency 99% Chlorocyclopentadienylbis(Triphenylphosphine)Ruthenium(II) 32993-05-8 Manufacturer

    Cas No: 32993-05-8

  • USD $ 0.1-0.1 / Gram

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  • Xi'an Xszo Chem Co., Ltd.
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32993-05-8 Usage

Description

Chlorocyclopentadienylbis(triphenylphosphine)ruthenium(II), also known as Ruthenium(II) chloride, is a transition metal complex with the chemical formula [CpRu(PPh3)2Cl]. It is an orange powder and is known for its catalytic properties in various chemical reactions.

Uses

Used in Pharmaceutical Industry:
Chlorocyclopentadienylbis(triphenylphosphine)ruthenium(II) is used as a catalyst in the synthesis of various pharmaceutical compounds, such as indoles, isoquinolines, and quinolines. These compounds are important building blocks for the development of new drugs and have potential applications in the treatment of various diseases.
Used in Chemical Synthesis:
In the field of chemical synthesis, Chlorocyclopentadienylbis(triphenylphosphine)ruthenium(II) is used as an efficient transfer hydrogenation catalyst. This application is crucial for the production of various organic compounds, as it allows for the selective reduction of functional groups without the need for external hydrogen sources.
Used in Research and Development:
Chlorocyclopentadienylbis(triphenylphosphine)ruthenium(II) is also utilized in research and development for the study of catalytic mechanisms and the development of new catalytic systems. Its unique properties make it a valuable tool for understanding and improving the efficiency of various chemical reactions.

Check Digit Verification of cas no

The CAS Registry Mumber 32993-05-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,9,9 and 3 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 32993-05:
(7*3)+(6*2)+(5*9)+(4*9)+(3*3)+(2*0)+(1*5)=128
128 % 10 = 8
So 32993-05-8 is a valid CAS Registry Number.
InChI:InChI=1/2C18H15P.C5H5.ClH.Ru/c2*1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18;1-2-4-5-3-1;;/h2*1-15H;1-5H;1H;/q;;;;-1/p+1/rC41H37ClP2Ru/c42-45(41-33-19-20-34-41,43(35-21-7-1-8-22-35,36-23-9-2-10-24-36)37-25-11-3-12-26-37)44(38-27-13-4-14-28-38,39-29-15-5-16-30-39)40-31-17-6-18-32-40/h1-34,41,43-44H

32993-05-8 Well-known Company Product Price

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  • TCI America

  • (C2201)  Cyclopentadienylbis(triphenylphosphine)ruthenium(II) Chloride  

  • 32993-05-8

  • 1g

  • 690.00CNY

  • Detail
  • TCI America

  • (C2201)  Cyclopentadienylbis(triphenylphosphine)ruthenium(II) Chloride  

  • 32993-05-8

  • 5g

  • 2,490.00CNY

  • Detail
  • Alfa Aesar

  • (46430)  Chloro(cyclopentadienyl)bis(triphenylphosphine)ruthenium(II) ethanol adduct   

  • 32993-05-8

  • 1g

  • 755.0CNY

  • Detail
  • Alfa Aesar

  • (46430)  Chloro(cyclopentadienyl)bis(triphenylphosphine)ruthenium(II) ethanol adduct   

  • 32993-05-8

  • 5g

  • 2960.0CNY

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  • Aldrich

  • (333158)  Chlorocyclopentadienylbis(triphenylphosphine)ruthenium(II)  

  • 32993-05-8

  • 333158-1G

  • 810.81CNY

  • Detail

32993-05-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name Chlorocyclopentadienylbis(triphenylphosphine)ruthenium(II)

1.2 Other means of identification

Product number -
Other names CpRu(PPh3)2Cl

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:32993-05-8 SDS

32993-05-8Relevant articles and documents

A VERSATILE ROUTE TO (η5-C5R5)RuL2X FROM ALLYLMETHYLRUTHENIUM COMPLEXES

Nagashima, Hideo,Yamaguchi, Keitaro,Mukai, Katsunori,Itoh, Kenji

, p. C20 - C22 (1985)

Divalent ruthenium complexes, (η5-C5R5)RuL2X (R=H, CH3; X=Br, Cl), are formed by thermal decomposition of (η5-C5R5)Ru(CH3)X(η3-C3H5) in the presence of several neutral ligands.

A new ruthenium cyclopentadienyl azole compound with activity on tumor cell lines and trypanosomatid parasites

Rodríguez Arce, Esteban,Sarniguet, Cynthia,Moraes, Tania S.,Vieites, Marisol,Tomaz, A. Isabel,Medeiros, Andrea,Comini, Marcelo A.,Varela, Javier,Cerecetto, Hugo,González, Mercedes,Marques, Fernanda,García, M. Helena,Otero, Lucía,Gambino, Dinorah

, p. 2923 - 2937 (2015)

(Chemical Equation Presented). As part of our efforts to develop organometallic ruthenium compounds bearing activity on both trypanosomatid parasites and tumor cells, a new Ru(II)-cyclopentadienyl clotrimazole complex, [RuCp(PPh3)2(C

The Kinatics of the Reaction of with Various Olefins

Alibrandi, Giuseppe,Mann, Brian E.

, p. 951 - 954 (1994)

A detailed kinetic investigation of the reaction of with cycloheptatriene, cyclohepta-1,3-diene, cyclooctatetraene, penta-1,4-diene, cycloocta-1,5-diene and dimethyl maleate, has been carried out spectrophotometrically in CH2Cl2 at 10 deg C.It is shown that the major mechanism is via dissociation of PPh3 to give which then reacts with the olefin.There is also a second mechanism involving direct attack of the olefin on .

Ashok, R. F. N.,Gupta, M.,Arulsamy, K. S.,Agarwala, U. C.

, p. 169 - 180 (1985)

Solvent- A nd anion-dependent rearrangement of fluorinated carbene ligands provides access to fluorinated alkenes

Hall, Lewis M.,Milner, Lucy M.,Hart, Sam J.,Whitwood, Adrian C.,Lynam, Jason M.,Slattery, John M.

supporting information, p. 17655 - 17659 (2019/12/23)

The construction of fluorocarbene ligands within the coordination sphere of transition metal complexes using sequential nucleophilic and electrophilic addition to a vinylidene complex is described. Reaction of [Ru(η5-C5H5)(dppe)(CCPhF)][N(SO2Ph)2] with [NMe4]F results in nucleophilic attack of fluoride at the metal-bound carbon of the vinylidene ligand to give alkenyl complex [Ru(η5-C5H5)(dppe)(-CFCFPh)]. Subsequent eletrophilic fluorination with N-fluorobenzenesulfonimide (NFSI) results in the formation of the fluorinated carbene complex [Ru(η5-C5H5)(dppe)(CF-CHFPh)][N(SO2Ph)2]. The fluorocarbene complexes undergo rearrangement to liberate free fluorinated alkenes, a process governed by the choice of solvent and anion, representing a new metal-mediated route to fluorinated alkenes from alkynes.

Syntheses of transition metal methoxysiloxides

Richers, Casseday P.,Bertke, Jeffery A.,Rauchfuss, Thomas B.

supporting information, p. 8756 - 8762 (2017/07/22)

The paper describes three methods for the preparation of methoxysiloxide complexes, a rare class of complexes of relevance to room temperature vulcanization (RTV) of polysiloxanes. The salt metathesis reaction involves the use of the recently described re

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