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Co(C5H5)(P(C6H5)3)CH2CH2CH2C(O) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

74656-85-2

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74656-85-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74656-85-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,6,5 and 6 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 74656-85:
(7*7)+(6*4)+(5*6)+(4*5)+(3*6)+(2*8)+(1*5)=162
162 % 10 = 2
So 74656-85-2 is a valid CAS Registry Number.

74656-85-2Relevant academic research and scientific papers

Synthesis, crystal and molecular structure, and chemistry of (μ-trimethylene)bis(η-cyclopentadienyl)bis(aμ-carbonyl)dicobalt, a five-membered dlcobaltacycle

Theopold, Klaus H.,Bergman, Robert G.

, p. 1571 - 1579 (2008/10/08)

Treatment of Na[CpCo(CO)]2 with l,n-dihaloalkanes leads in certain cases to double alkylation, giving dinuclear metallacycles containing two adjacent cobalt atoms. This paper reports the synthesis and study of several such systems and an in-depth investigation of the five-membered dimetallacycle 1 prepared from 1,3-diiodopropane. The molecular structure of 1 was determined by X-ray diffraction, using 1016 reflections (R = 2.47). The crystals were orthorhombic (space group Fdd2), with unit-cell parameters a = 16.7983 ?, b = 45.576 ?, c = 6.9565 ?. The complex has an open envelope ring structure, with a dihedral angle of 32.9°; the Co-Co bond distance is 2.413 ?. Thermolysis of 1 (80-100°) gives cyclopropane and propene. Reaction of 1 with CO or phosphines (L) occurs at lower temperature, leading to a product distribution which is dependent upon the concentration of L. At low [L], the reaction leads to cyclopropane mixed with a small amount of propene and CpCo(L)(CO). High [L] produces CpCo(L)(CO) and mononuclear metallacyclopentanones 6, 7, or 8 depending on the entering ligand. Thermolysis of the metallacyclopentanones leads again to cyclopropane and propene rather than to cyclobutanone. Kinetic and isotope labeling studies on the reaction of 1 with dative ligands suggest a mechanism involving initial formation of dicobaltacyclohexanones A and B. B then is postulated to rearrange to a mononuclear carbonylmetallacyclobutane complex (C) which can either eliminate C3 hydrocarbons or undergo CO insertion, leading to metallacyclopentanone.

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