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1,4-Naphthalenedione, 2-chloro-3-[(2,4-dinitrophenyl)amino]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

488128-98-9

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488128-98-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 488128-98-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,8,8,1,2 and 8 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 488128-98:
(8*4)+(7*8)+(6*8)+(5*1)+(4*2)+(3*8)+(2*9)+(1*8)=199
199 % 10 = 9
So 488128-98-9 is a valid CAS Registry Number.

488128-98-9Downstream Products

488128-98-9Relevant academic research and scientific papers

Palladium-catalyzed amination of 2,3-dichloro-1,4-naphthoquinone with nitroarylamines

Wang, Xiao-Lei,Zheng, Xiu-Fang,Reiner, John

, p. 942 - 944 (2006)

A convenient one-step synthesis of 2-[(nitroaryl)amino]-3-chloro-1,4- naphthoquinones is reported. The direct amination of 2,3-dichloro-1,4- naphthoquinone with nitro-substituted aryl amines is catalyzed by PdCl 2(dppf)/dppf in the presence of

Thermolysis of 2-azido-3-(R-anilino)-1,4-naphthoquinones. Nitrene insertion versus hydrogen abstraction

Cárdenas-Chaparro, Agobardo,Leyva, Elisa,Loredo-Carrillo, Silvia E.,Martínez-Richa, Antonio,Platz, Matthew S.

, (2020/03/03)

2-chloro-3-(R-anilino)-1,4-naphthoquinones react with sodium azide upon refluxing in DMF. The thermochemistry of 2-azido-3-(R-anilino)-1,4-naphthoquinone is strongly modified by the substituent on aniline. Having an strong electron-donor like O-R results

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 (2017/02/15)

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.

Synthesis of novel 2-(fluoroanilino)-3-(2,4-dinitroanilino) derivatives of 1,4-naphthoquinone

Leyva, Elisa,Baines, Kim M.,Espinosa-González, Claudia G.,López, Lluvia I.,Magaldi-Lara, Diego A.,Leyva, Socorro

, p. 5248 - 5251 (2015/08/19)

Several novel 2-(fluoroanilino)-3-(2,4-dinitroanilino) derivatives of 1,4-naphthoquinone have been synthesized in good to excellent yields. First, 2-chloro-3-(2,4-dinitroanilino)-1,4-naphthoquinone was prepared in two steps beginning with the reaction of

Direct nitration of 3-arylamino-2-chloro-1,4-naphthoquinones

Win, Thida,Yerushalmi, Sarit,Bittner, Shmuel

, p. 1631 - 1634 (2007/10/03)

A convenient two-step synthesis of mononitro and dinitro derivatives of the title compounds is reported. The Michael type addition of aromatic amines to 2,3-dichloro-1,4-naphthoquinone, is followed by mixed acids nitration to yield nitro aromatic quinones

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