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N,N'-bis(2,2-diphenylethyl)-1,2-hydrazidocarboxamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1240158-45-5

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1240158-45-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1240158-45-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,0,1,5 and 8 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1240158-45:
(9*1)+(8*2)+(7*4)+(6*0)+(5*1)+(4*5)+(3*8)+(2*4)+(1*5)=115
115 % 10 = 5
So 1240158-45-5 is a valid CAS Registry Number.

1240158-45-5Downstream Products

1240158-45-5Relevant academic research and scientific papers

Azodicarboxamides as template binding motifs for the building of hydrogen-bonded molecular shuttles

Berna, Jose,Alajarin, Mateo,Orenes, Raul-Angel

, p. 10741 - 10747 (2010)

Azodicarboxamides (R2NCON-NCONR2) are shown to act as new templates for the assembly of unprecedented azo-functionalized hydrogen-bond-assembled [2]rotaxanes. Moreover, these binding sites can be reversibly and efficiently interconverted with their hydrazo forms through a hydrogenation-dehydrogenation strategy of the nitrogen-nitrogen bond. This novel chemically switchable control element has been implemented in stimuli-responsive molecular shuttles that work through a reversible azo/hydrazo interconversion, producing large amplitude net positional changes with a good discrimination between the binding sites of the macrocycle in both states of the shuttle. These molecular shuttles are able to operate by two different mechanisms: in a discrete mode through two reversible and independent chemical events and, importantly, in a continuous regime through a catalyzed ester bond formation reaction in which the shuttle acts as an organocatalyst. In this latter, the incorporation of both states of the shuttle into this simple chemical reaction network promotes a dynamic translocation of the macrocycle between two nitrogen and carbon-based stations of the thread allowing an energetically uphill esterification process to take place.

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