51076-59-6 Usage
General Description
2-(1H-imidazol-2-yl)-malonaldehyde is a chemical compound that consists of an imidazole ring attached to a malonaldehyde moiety. Malonaldehyde is a reactive molecule that can form adducts with proteins and nucleic acids, potentially causing damage to cellular structures. The imidazole ring in this compound provides a nitrogen-containing heterocyclic structure that can participate in various chemical reactions. The compound may have potential applications in organic synthesis, medicinal chemistry, and biochemical research due to its unique structure and reactivity. Overall, 2-(1H-imidazol-2-yl)-malonaldehyde is a novel compound with potential use in various fields of chemistry and biology.
Check Digit Verification of cas no
The CAS Registry Mumber 51076-59-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,0,7 and 6 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 51076-59:
(7*5)+(6*1)+(5*0)+(4*7)+(3*6)+(2*5)+(1*9)=106
106 % 10 = 6
So 51076-59-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H6N2O2/c9-3-5(4-10)6-7-1-2-8-6/h1-5H,(H,7,8)
51076-59-6Relevant articles and documents
1,8-Naphthyridine compounds
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, (2008/06/13)
There is described 1,8-naphthyridin-2(1H)-one compounds with bronchodilating and hypotensive properties prepared by reaction of 2,6-diaminopyridine with an appropriate β-diketone providing a 2-aminonaphthyridine compound which upon treatment with nitrous acid is converted to the 2-oxo product. Alternatively, an appropriate β-diketone can be reacted with an alkyl alkoxycarbonylacetimidate, the alkyl 2-aminonicotinate thus formed converted to the hydrazide, which upon treatment with a sulfonyl halide forms the N-sulfonyl hydrazide derivative. This intermediate is reacted with an alkali metal carbonate to provide the 2-aminonicotinaldehyde which upon reaction with an ester of a substituted aliphatic carboxylic acid provides the desired product. In some cases the aminonicotinaldehyde is generated in situ in the presence of the ester thereby giving the desired product in one step from the N-sulfonyl hydrazide derivative.
