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N-benzylquinoline-6-carboxamide is a chemical compound with the molecular formula C18H16N2O. It is a derivative of quinoline-6-carboxamide, featuring a benzyl group attached to the nitrogen atom. N-benzylquinoline-6-carboxamide is known for its potential applications in medicinal chemistry, particularly as a precursor in the synthesis of various biologically active molecules. It has been studied for its potential anti-cancer properties and is also used in the development of new drugs targeting specific enzymes or receptors. The compound's structure allows for further functionalization and modification, making it a versatile building block in organic synthesis and drug design.

6843-60-3

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6843-60-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6843-60-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,8,4 and 3 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6843-60:
(6*6)+(5*8)+(4*4)+(3*3)+(2*6)+(1*0)=113
113 % 10 = 3
So 6843-60-3 is a valid CAS Registry Number.

6843-60-3Downstream Products

6843-60-3Relevant academic research and scientific papers

Highly selective synthesis of 6-glyoxylamidoquinoline derivatives via palladium-catalyzed aminocarbonylation

Bényei, Attila,Chniti, Sami,Kollár, László,Takács, Attila

supporting information, (2021/12/29)

The aminocarbonylation of 6-iodoquinoline has been investigated in the presence of large series of amine nucleophiles, providing an efficient synthetic route for producing various quinoline-6-carboxamide and quinoline-6-glyoxylamide derivatives. It was shown, after detailed optimization study, that the formation of amides and ketoamides is strongly influenced by the reaction conditions. Performing the reactions at 40 bar of carbon monoxide pressure in the presence of Pd(OAc)2/2 PPh3, the corresponding 2-ketocarboxamides were formed as major products (up to 63%). When the monodentate triphenylphosphine was replaced by the bidentate XantPhos, the quinoline-6-carboxamide derivatives were synthesized almost exclusively under atmospheric conditions (up to 98%). The isolation and characterization of the new carbonylated products of various structures were also accomplished. Furthermore, the structure of three new mono-and double-carbonylated compounds were unambiguously established by using a single-crystal XRD study.

SECONDARY 8-HYDROXYQUINOLINE-7-CARBOXAMIDE DERIVATIVES FOR USE AS ANTIFUNGAL AGENTS

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Page/Page column 28, (2011/07/30)

The present invention provides secondary 8-hydroxyquinoiine-7-carboxamide derivatives of general formula (I) and pharmaceutically acceptable salts thereof. These compounds are useful as antifungal agents. Specifically, these compounds were tested against Tricophyton Rubrum, Tricophyton Mentagrophytes, Aspergillus Niger and Scopulahopsis Brevicaulis. These compounds are active against Candida species such as Candida Albicans and Candida Glabrata.

AGRICULTURAL COMPOSITION FOR CONTROLLING OR PREVENTING PLANT DISEASES CAUSED BY PLANT PATHOGENIC MICROBES

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Page/Page column 69, (2008/12/08)

An agricultural composition comprising an amide compound represented by the following formula (I), a salt thereof, or a hydrate thereof is effective for controlling or preventing plant diseases caused by plant pathogenic microbes when an effective amount

Antithrombotic phenylalkyl derivatives

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, (2008/06/13)

Antithrombotic phenylalkyl derivatives of the formula Exemplary compounds are: (a) 1-[3-(4-amidino-phenyl)propionyl]-6-(4-fluoro-phenylsulphonamido)-1,2,3,4-tetrahydro-quinoline, (b) 1-[3-(4-amidino-phenyl)propionyl]-6-butylsulphonamido-1,2,3,4-tetrahydro

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