Cas 1290573-54-4,2,2'-[(E)-ethene-1,2-diylbis(pyridinio-4,1-diylmethylene)]dibenzenesulfonate

1290573-54-4

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Basic information

Product Name: 2,2'-[(E)-ethene-1,2-diylbis(pyridinio-4,1-diylmethylene)]dibenzenesulfonate
Synonyms: 2,2'-[(E)-ethene-1,2-diylbis(pyridinio-4,1-diylmethylene)]dibenzenesulfonate
CAS NO:1290573-54-4
Molecular Formula:
Molecular Weight: 522.602
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 2,2'-[(E)-ethene-1,2-diylbis(pyridinio-4,1-diylmethylene)]dibenzenesulfonate(CAS DataBase Reference)
NIST Chemistry Reference: 2,2'-[(E)-ethene-1,2-diylbis(pyridinio-4,1-diylmethylene)]dibenzenesulfonate(1290573-54-4)
EPA Substance Registry System: 2,2'-[(E)-ethene-1,2-diylbis(pyridinio-4,1-diylmethylene)]dibenzenesulfonate(1290573-54-4)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1290573-54-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1290573-54-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,9,0,5,7 and 3 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1290573-54:
(9*1)+(8*2)+(7*9)+(6*0)+(5*5)+(4*7)+(3*3)+(2*5)+(1*4)=164
164 % 10 = 4
So 1290573-54-4 is a valid CAS Registry Number.

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1290573-54-4Relevant academic research and scientific papers

Pseudorotaxane complexes between viologen vinylogues and cucurbit[7]uril: New prototype of photocontrolled molecular machine

Vedernikov, Artem I.,Lobova, Natalia A.,Kuz'mina, Lyudmila G.,Howard, Judith A.K.,Strelenko, Yuri A.,Alfimov, Michael V.,Gromov, Sergey P.

, p. 114 - 121 (2011)

Dibetaines of unsaturated viologen analogues that form supramolecular complexes with cucurbit[7]uril were synthesized. The pseudorotaxane structure and stability of the complexes were established by UV/Vis and 1H NMR spectroscopy and by X-ray d

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