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trans-carbonylhydridotris(triphenylphosphine)cobalt(I) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

53729-69-4

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53729-69-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53729-69-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,7,2 and 9 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 53729-69:
(7*5)+(6*3)+(5*7)+(4*2)+(3*9)+(2*6)+(1*9)=144
144 % 10 = 4
So 53729-69-4 is a valid CAS Registry Number.

53729-69-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name trans-carbonylhydridotris(triphenylphosphine)cobalt(I)

1.2 Other means of identification

Product number -
Other names -

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:53729-69-4 SDS

53729-69-4Downstream Products

53729-69-4Relevant academic research and scientific papers

Carbon-Oxygen Bond Cleavage of Esters Promoted by Hydrido and Alkylcobalt(I) Complexes Having Triphenylphosphine Ligands. Isolation of an Insertion Intermediate and Molecular Structure of Phenoxotris(triphenylphosphine)cobalt(I)

Hayashi, Yoshinori,Yamamoto, Takakazu,Yamamoto, Akio,Komiya, Sanshiro,Kushi, Yoshihiko

, p. 385 - 391 (2007/10/02)

Carbon-oxygen bonds in aryl and alkyl carboxylates (R'COOR) are selectively cleaved by CoH(N2)(PPh3)3, and carboxylic esters R'COOCH2R' are formed by a Tischchenko type dimerization of aldehyde R'CHO, whereas the reaction of CoMe(PPh3)3 with the esters yields ketones R'COMe.The reaction products are accounted for by assuming insertion of the ester C=O double bond into the Co-H or Co-Me bond, followed by abstraction of the β-alkoxo group by cobalt.The intermediate (β-(ethoxy)alkoxo)cobalt(I) complex Co(OCH(CF3)OEt)(PPh3)3 has been isolated in the reaction of CoH(N2)(PPh3)3 with ethyl trifluoroacetate as well as by alcoholysis of CoH(N2)(PPh3)3 with CF3CH(OEt)OH.Treatment of CoH(N2)(PPh3)3 with phenyl acetate affords a tetrahedral phenoxocobalt(I) complex, Co(OPh)(PPh3)3.Crystals of the complex are monoclinic, space group P21/c, with a = 13.142(2) Angstroem, b = 19.661(3) Angstroem, c = 18.714(3) Angstroem, and β = 91.49(3) degree.Block-diagonal least-squares refinement leads to R = 0.075 and Rw = 0.081 for 2966 reflections.The molecular structure of the complexe consists of a tetrahedron with an O-bonded phenoxo group and three PPh3 ligands; the average Co-P distance is 2.320(4) Angstroem and Co-O 1.900(9) Angstroem, and the average P-Co-P angle is 109.9(1) degree, P-Co-O 109.1(4) degree, and Co-O-C 138.2(9) degree, respectively.

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