Cas 1246169-07-2,(4,4')-4,4'-(2,2'-(1,4-phenylene)bis(hydrazin-2-yl-1-ylidene))bis-1-phenylpyrazolidine-3,5-dione

1246169-07-2

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Basic information

Product Name: (4,4')-4,4'-(2,2'-(1,4-phenylene)bis(hydrazin-2-yl-1-ylidene))bis-1-phenylpyrazolidine-3,5-dione
Synonyms: (4,4')-4,4'-(2,2'-(1,4-phenylene)bis(hydrazin-2-yl-1-ylidene))bis-1-phenylpyrazolidine-3,5-dione
CAS NO:1246169-07-2
Molecular Formula:
Molecular Weight: 482.458
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: (4,4')-4,4'-(2,2'-(1,4-phenylene)bis(hydrazin-2-yl-1-ylidene))bis-1-phenylpyrazolidine-3,5-dione(CAS DataBase Reference)
NIST Chemistry Reference: (4,4')-4,4'-(2,2'-(1,4-phenylene)bis(hydrazin-2-yl-1-ylidene))bis-1-phenylpyrazolidine-3,5-dione(1246169-07-2)
EPA Substance Registry System: (4,4')-4,4'-(2,2'-(1,4-phenylene)bis(hydrazin-2-yl-1-ylidene))bis-1-phenylpyrazolidine-3,5-dione(1246169-07-2)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1246169-07-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1246169-07-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,6,1,6 and 9 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1246169-07:
(9*1)+(8*2)+(7*4)+(6*6)+(5*1)+(4*6)+(3*9)+(2*0)+(1*7)=152
152 % 10 = 2
So 1246169-07-2 is a valid CAS Registry Number.

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1246169-07-2Relevant academic research and scientific papers

Simple route to a novel class of pyrazolidine-3,5-dione based azo dyes

Isaad, Jalal,Perwuelz, Anne

, p. 5328 - 5332 (2010)

We report an easiest synthesis strategy of a new class of synthetic dyes by coupling of functionalized pyrazolidine-3,5-dione derivatives via diazotization reaction with aromatic diamine for the azoic dyes or via dimerization reaction to synthesize the H chromophore dyes. Electron delocalization between the two coupled components has been studied using UV-vis spectroscopy, infrared, and NMR spectroscopy. In addition, the formation mechanism of such compounds has been discussed.

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