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2-chloro-3-(2,4-difluoroanilino)-1,4-naphthoquinone is a complex organic chemical compound with the molecular formula C16H6ClF2NO2. It is characterized by a naphthoquinone core, which is a type of quinone with a fused benzene ring, and features a chlorine atom at the 2-position, a 2,4-difluoroaniline group attached at the 3-position, and a carbonyl group at both the 1 and 4 positions. 2-chloro-3-(2,4-difluoroanilino)-1,4-naphthoquinone is known for its potential applications in the synthesis of pharmaceuticals and agrochemicals, particularly as an intermediate in the production of certain anticancer drugs. Its chemical structure endows it with specific reactivity and properties that make it valuable in medicinal chemistry and chemical research.

3859-78-7

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3859-78-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3859-78-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,5 and 9 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3859-78:
(6*3)+(5*8)+(4*5)+(3*9)+(2*7)+(1*8)=127
127 % 10 = 7
So 3859-78-7 is a valid CAS Registry Number.

3859-78-7Downstream Products

3859-78-7Relevant academic research and scientific papers

Synthesis and studies of the antifungal activity of 2-anilino-/2,3-dianilino-/2-phenoxy- and 2,3-diphenoxy-1,4-naphthoquinones

Leyva, Elisa,López, Lluvia I.,de la Cruz, Ramón F. García,Espinosa-González, Claudia G.

, p. 1813 - 1827 (2017)

Several synthetic and natural naphthoquinone derivatives have been associated with antifungal activity. Candida albicans is a fungus that is known to exist in the normal human flora, but under certain conditions it can cause mild to fatal infections. Its pathogenicity has been associated with fungus conversion from cellular yeast to filamentous form Y–M. Inhibition of this process by several anilino-, dianilino-, phenoxy-, and diphenoxy-1,4-naphthoquinones was investigated in order to find some correlation between structure, redox properties and biological activity.

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