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[1,2,4]Triazolo[4,3-a][1,8]naphthyridine-6-carboxamide, N,N-diethyl-9-(1-methylethyl)-5-(phenylamino)is a complex chemical compound that belongs to the family of naphthyridine carboxamides. It is characterized by a triazolo ring fused to a naphthyridine ring, with a carboxamide group at position 6. [1,2,4]Triazolo[4,3-a][1,8]naphthyridine-6-carboxamide,
N,N-diethyl-9-(1-methylethyl)-5-(phenylamino)also features diethyl and isopropyl groups at position 9, and a phenylamino group at position 5 of the naphthyridine ring. Given its structural features and the presence of an amide group, which is commonly found in bioactive molecules, it may have potential pharmaceutical applications. However, further research is required to explore its biological activities and potential uses.

848820-49-5

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848820-49-5 Usage

Uses

Used in Pharmaceutical Industry:
[1,2,4]Triazolo[4,3-a][1,8]naphthyridine-6-carboxamide, N,N-diethyl-9-(1-methylethyl)-5-(phenylamino)is used as a potential pharmaceutical candidate for various applications due to its unique structural features and the presence of an amide group. [1,2,4]Triazolo[4,3-a][1,8]naphthyridine-6-carboxamide,
N,N-diethyl-9-(1-methylethyl)-5-(phenylamino)-'s potential uses may include the development of new drugs targeting specific biological pathways or receptors, as well as the enhancement of existing drug therapies.
Used in Research and Development:
In the field of research and development, [1,2,4]Triazolo[4,3-a][1,8]naphthyridine-6-carboxamide, N,N-diethyl-9-(1-methylethyl)-5-(phenylamino)can be utilized as a starting point for the synthesis of novel compounds with potential applications in various industries, including pharmaceuticals, agrochemicals, and materials science. Its unique structure and functional groups may provide a foundation for the development of new molecules with improved properties and enhanced biological activities.
Used in Drug Design and Optimization:
[1,2,4]Triazolo[4,3-a][1,8]naphthyridine-6-carboxamide, N,N-diethyl-9-(1-methylethyl)-5-(phenylamino)can be employed in drug design and optimization processes to identify new lead compounds or improve the properties of existing drug candidates. Its structural features and the presence of an amide group may facilitate the development of molecules with enhanced potency, selectivity, and pharmacokinetic properties, ultimately leading to more effective therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 848820-49-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,8,8,2 and 0 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 848820-49:
(8*8)+(7*4)+(6*8)+(5*8)+(4*2)+(3*0)+(2*4)+(1*9)=205
205 % 10 = 5
So 848820-49-5 is a valid CAS Registry Number.

848820-49-5Downstream Products

848820-49-5Relevant academic research and scientific papers

1,8-Naphthyridines V. Novel N-substituted 5-amino-N,N-diethyl-9-isopropyl [1,2,4]triazolo[4,3-a] [1,8]naphthyridine-6-carboxamides, as potent anti-inflammatory and/or analgesic agents completely devoid of acute gastrolesivity

Grossi, Giancarlo,Di Braccio, Mario,Roma, Giorgio,Ballabeni, Vigilio,Tognolini, Massimiliano,Barocelli, Elisabetta

, p. 155 - 165 (2007/10/03)

Most N,N-disubstituted 5-amino-N,N-diethyl-9-isopropyl [1,2,4]triazolo[4,3- a] [1,8]naphthyridine-6-carboxamides 9 (compounds 9a, c-i) and the N-monosubstituted one 8c were obtained by treating with excess amine the corresponding 5-chloroderivative 7a, wh

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