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2,2'-[(E)-1,2-Ethenediyl]difuran, also known as 2,2'-(1,2-ethenediyl)bisfuran or simply ethylenediylbisfuran, is an organic compound characterized by a unique structure that features two furan rings connected by a vinyl (ethenyl) bridge. Furan is a heterocyclic compound with a five-membered ring containing four carbon atoms and one oxygen atom. In this specific compound, the vinyl bridge (E)-1,2-ethenediyl links the two furan rings in an E configuration, which refers to the geometric arrangement of the double bond where the substituents are on opposite sides of the bond. 2,2'-[(E)-1,2-Ethenediyl]difuran is of interest in organic chemistry and material science due to its potential applications in the synthesis of various polymers and as a building block for more complex organic molecules.

1439-19-6

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1439-19-6 Usage

Structure

Two furan rings connected by a carbon-carbon double bond

Type of compound

Conjugated diene

Usage

Building block in organic synthesis, potential applications in materials science and pharmaceuticals

Synthesis

Starting material for the synthesis of various organic compounds

Biological activities

Studied for potential biological activities

Versatility

Potential applications in various fields of chemistry

Check Digit Verification of cas no

The CAS Registry Mumber 1439-19-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,3 and 9 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1439-19:
(6*1)+(5*4)+(4*3)+(3*9)+(2*1)+(1*9)=76
76 % 10 = 6
So 1439-19-6 is a valid CAS Registry Number.

1439-19-6Relevant academic research and scientific papers

Methods to delay deactivation of zeolites on furan acylation: Continuous liquid-phase technology and solvent effects

Xiong, Yuannan,Chen, Wenqi,Ma, Jianjun,Chen, Zhihua,Zeng, Aiwu

, p. 103695 - 103702 (2015/12/23)

The continuous liquid-phase Friedel-Crafts acylation of furan with acetic anhydride was first carried out in a fixed-bed reactor over an H-beta zeolite. A three-level, four-variable Box-Behnken design combined with response surface methodology was employed to determine the optimal acylation conditions, and the accuracy of the model was verified by validation experiments. In this study, it was found that lower liquid velocity and stronger polarity of the solvent were conducive to enhancing the catalytic activity and stability of the H-beta zeolite. The reaction was limited by the acid sites being poisoned due to the adsorption of the by-product and pore blockage. Moreover, the carbon deposit was proved to be the main reason for the deactivation of the H-beta zeolite by using GC-MS, 13C NMR MAS, 27Al NMR MAS, TG/DTG and NH3-TPD.

THERMOLYSIS OF SODIUM SALTS OF TOSYLHYDRAZONES OF SOME HETEROCYCLIC ALDEHYDES IN THE PRESENCE OF SILVER CHROMATE: 1,3 NC MIGRATION OF TOSYL GROUP

Saito, Katsuhiro,Ishihara, Hiraku

, p. 1891 - 1898 (2007/10/02)

The thermal decompositions of sodium salts of tosylhydrazones of furfural, thiophene-2-aldehyde, 1-methylpyrrole-2-aldehyde, and pyridine-2-aldehyde in the presence of silver chromate gave 2-furyl(p-toluenesulfonyl)methane, thiophene-2-(p-toluenesulfonyl)methane, 1-methylpyrrole-2-(p-toluenesulfonyl)methane, and pyridine-2-(p-toluenesulfonyl)methane, respectively, via 1,3 NC migration of tosyl group.The same type of reactions with sodium salts of tosylhydrazones of thiophene-3-aldehyde, pyridine-3-aldehyde, and pyridine-4-aldehyde also afforded the corresponding p-toluenesulfonylmethanes but the yields were slightly lower comparing to the above cases.

THERMOLYSIS OF SODIUM SALT OF FURFURAL TOSYLHYDRAZONE IN THE PRESENCE OF SILVER CHROMATE: FORMATION OF 2-FURYL(p-TOLUENESULFONYL)METHANE VIA 1,3N->C MIGRATION OF TOSYL GROUP

Saito, Katsuhiro,Ishihara, Hiraku

, p. 1291 - 1294 (2007/10/02)

The thermal decomposition of sodium salt of furfural tosylhydrazone in diglyme in the presence of silver chromate afforded trans-1,2-di(2-furyl)ethylene and 2-furyl(p-toluenesulfonyl)methane.The former product is formed via (2-furyl)methylene, while the l

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