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87668-43-7

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87668-43-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87668-43-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,6,6 and 8 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 87668-43:
(7*8)+(6*7)+(5*6)+(4*6)+(3*8)+(2*4)+(1*3)=187
187 % 10 = 7
So 87668-43-7 is a valid CAS Registry Number.

87668-43-7Upstream product

87668-43-7Downstream Products

87668-43-7Relevant academic research and scientific papers

The 15N NMR Spectra of Macrocyclic Compounds Containing the Ferrocene Unit

Hall, C. Dennis,Bell, Alan P.,Denney, Dorothy C.

, p. 94 - 95 (1981)

The synthesis of a 15N enriched macrocycle containing the ferrocene unit is described, and the 15N NMR spectra of the macrocycle and those of its complexes with some metallic cations are reported.

Synthesis, N.m.r. Spectra, and Structure of Macrocyclic Compounds containing the Ferrocene Unit

Hammond, Philip J.,Bell, Alan P.,Hall, C. Dennis

, p. 707 - 715 (2007/10/02)

The condensation of 1,1'-bis(chlorocarbonyl)ferrocene with diaza-18-crown-6 gives 1,1'-(1,4,10,13-tetraoxa-7,16-diazacyclo-octadecane-7,16-diyldicarbonyl)ferrocene (5) together with its dimer 1,1'':1',1'''-bis-(1,4,10,13-tetraoxa-7,16-diazacyclo-octadecane-7,16-diyldicarbonyl)bisferrocene (6) and the separation and isolation of these compounds are described.High resolution 1H and 13C n.m.r. spectra using homo- and hetero-nuclear decoupling techniques allow a complete assignment of the spectral data for (5) and (6) and lead to a proposal of a structure for (5) involving a trans-disposition of the amide carbonyl groups.Variable-temperature n.m.r. data on (6) reveal two distinct dynamic processes within the molecule involving rotation about the ferrocene-carbonyl bond (ΔG=50 kJ mol-1, Tc=-10 deg C) and rotation about the N-CO bond (ΔG=67 kJ mol-1, Tc=+60 deg C).The preparation, 1H and 13C n.m.r. data of monocyclic compounds containing the ferrocene unit (13a-c), (14) and (15) are also described and the details of the synthesis of an 15N-labelled analogue of (13c), the macrocycle (16), are reported.

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