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1-oxo-1,2-dihydrobenzo[b]-1,6-naphthyridine is a chemical compound with the molecular formula C12H9NO and a molecular weight of 183.21 g/mol. It belongs to the class of organic compounds known as naphthyridines, which are fused heterocyclic compounds consisting of a benzene ring and a pyridine ring. This specific compound features a benzene ring fused to a dihydro-1,6-naphthyridine ring, with a carbonyl group (C=O) at the 1-position. It is an important intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly those with potential applications as antimicrobial, anticancer, and anti-inflammatory agents. The compound is typically synthesized through various chemical reactions, such as condensation or cyclization, and can be further functionalized to yield a range of derivatives with diverse biological activities.

74990-58-2

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74990-58-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74990-58-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,9,9 and 0 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 74990-58:
(7*7)+(6*4)+(5*9)+(4*9)+(3*0)+(2*5)+(1*8)=172
172 % 10 = 2
So 74990-58-2 is a valid CAS Registry Number.

74990-58-2Downstream Products

74990-58-2Relevant academic research and scientific papers

New approach to the synthesis of 4-amino-2-pyridone and 1-phenyl-1,6-naphthyridinone derivatives based on substituted 3-and 5-formyl-2-pyridones

Tugusheva,Alekseeva,Shashkov,Granik

, p. 1470 - 1474 (2006)

The reactions of 3-cyano-3(5)-formyl-2-oxo-4-(phenylamino)-1,2- dihydropyridines with CH acids were studied. The previously unknown fused 2-pyridone derivatives containing the 4-aminopyridine fragment were synthesized by the Knoevenagel reaction.

Synthesis and functionalization of 4-arylamino-2-pyridone derivatives

Tugusheva,Alekseeva,Shashkov,Chernyshev,Granik

, p. 1475 - 1486 (2007/10/03)

New approaches to the synthesis of the previously unknown pyrimidine, 4-amino-2-pyridone, and 4-aminopyridine derivatives were developed based on the reactions of enaminoamides with dimethylformamide dimethyl acetal. New structural modifications of 4-amin

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