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6,7-diethoxy-3-ethoxycarbonyl-4(1H)-quinolone is a complex organic compound characterized by its quinolone structure, which is a type of heterocyclic compound with a benzene ring fused to a pyridine ring. This specific compound features two ethoxy groups at the 6 and 7 positions, an ethoxycarbonyl group at the 3 position, and a 4(1H)-quinolone functional group. The ethoxycarbonyl group suggests the presence of an ester, which can be hydrolyzed to yield a carboxylic acid and an alcohol. The compound's structure and functional groups endow it with potential applications in pharmaceuticals, agrochemicals, or as intermediates in organic synthesis. Its chemical properties and reactivity are influenced by the presence of these functional groups, making it a compound of interest for further study and potential development.

1698-92-6

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1698-92-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1698-92-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,9 and 8 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1698-92:
(6*1)+(5*6)+(4*9)+(3*8)+(2*9)+(1*2)=116
116 % 10 = 6
So 1698-92-6 is a valid CAS Registry Number.

1698-92-6Downstream Products

1698-92-6Relevant academic research and scientific papers

4(1H)-quinolone derivatives

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, (2008/06/13)

Quinolone derivatives having a quinolone structure: STR1 where Yo is O or S are disclosed, which are useful as cardiotonic agents. Typical examples of the quinolone derivatives include: 6,7-dimethoxy-4 (1H) quinolone (compound 6) and 5-hydroxy-6-methoxy-4(1H) quinolone (compound 1) as typical compounds of the formulae[I] and [I'], respectively, shown in the specification.

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