Cas 1361327-63-0,3-chloro-N-(3-chlorobenzoyl)-N-(3-chloro-1,4-dioxo-1,4-dihydronaphthalen-2-yl)-benzamide

1361327-63-0

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Basic information

Product Name: 3-chloro-N-(3-chlorobenzoyl)-N-(3-chloro-1,4-dioxo-1,4-dihydronaphthalen-2-yl)-benzamide
Synonyms: 3-chloro-N-(3-chlorobenzoyl)-N-(3-chloro-1,4-dioxo-1,4-dihydronaphthalen-2-yl)-benzamide
CAS NO:1361327-63-0
Molecular Formula:
Molecular Weight: 484.723
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 3-chloro-N-(3-chlorobenzoyl)-N-(3-chloro-1,4-dioxo-1,4-dihydronaphthalen-2-yl)-benzamide(CAS DataBase Reference)
NIST Chemistry Reference: 3-chloro-N-(3-chlorobenzoyl)-N-(3-chloro-1,4-dioxo-1,4-dihydronaphthalen-2-yl)-benzamide(1361327-63-0)
EPA Substance Registry System: 3-chloro-N-(3-chlorobenzoyl)-N-(3-chloro-1,4-dioxo-1,4-dihydronaphthalen-2-yl)-benzamide(1361327-63-0)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1361327-63-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1361327-63-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,1,3,2 and 7 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1361327-63:
(9*1)+(8*3)+(7*6)+(6*1)+(5*3)+(4*2)+(3*7)+(2*6)+(1*3)=140
140 % 10 = 0
So 1361327-63-0 is a valid CAS Registry Number.

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1361327-63-0Relevant academic research and scientific papers

Method for inhibiting Trypanosoma cruzi

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Page/Page column 22; 23; 24, (2016/09/26)

Methods are provided to inhibit proliferation of Trypanosoma cruzi with imido-substituted 1,4-naphthoquinones, including novel compounds. Administering an imido-substituted 1,4-naphthoquinone can be used to provide prophylaxis or treatment to a patient in

METHOD FOR INHIBITING TRYPANSOMA CRUZI

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Paragraph 27; 28; 29; 30, (2013/03/26)

In its broadest aspect, a method for treating a mammalian patient at risk or suffering from a disease caused by a kinetoplastid parasite comprises administering to such subject an effective kinetoplasticidal amount of an imido-substituted 1,4- naphthoquin

METHODS FOR TREATING LEISHMANIASIS

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Page/Page column 27, (2013/06/05)

Methods are provided to inhibit proliferation of Leishmania parasites, and in particular Leishmania donovani with imido-substituted 1,4-naphthoquinones, including novel compounds. Administering an imido-substituted 1,4-naphthoquinone can be used to provide prophylaxis or treatment to a patient in need of treatment against leishmaniasis disease.

Synthesis and characterization of novel unsymmetrical and symmetrical 3-halo- or 3-methoxy-substituted 2-dibenzoylamino-1,4-naphthoquinone derivatives

Brandy, Yakini,Brandy, Nailah,Akinboye, Emmanuel,Lewis, Malik,Mouamba, Claudia,MacK, Seshat,Butcher, Ray J.,Anderson, Alan J.,Bakare, Oladapo

, p. 1973 - 1984 (2013/04/10)

Symmetrical and unsymmetrical 3-halo- or 3-methoxy- substituted 2-dibenzoylamino- 1,4-naphthoquinone analogs were synthesized with an average yield of 45% via sodium hydride promoted bis-acylation of 2-amino-3-chloro-1,4- naphthoquinone, 2-amino-3-bromo- 1,4-naphthoquinone and 2-amino-3-methoxy-1,4- naphthoquinone.

Antitrypanosomal activities and cytotoxicity of some novel imidosubstituted 1,4-naphthoquinone derivatives

Khraiwesh, Mozna H.,Lee, Clarence M.,Brandy, Yakini,Akinboye, Emmanuel S.,Berhe, Solomon,Gittens, Genelle,Abbas, Muneer M.,Ampy, Franklin R.,Ashraf, Mohammad,Bakare, Oladapo

experimental part, p. 27 - 33 (2012/07/02)

The antitrypanosomal activities, cytotoxicity, and selectivity indices of eleven imido-substituted 1,4-naphthoquinone derivatives and nifurtimox have been studied. Compared to nifurtimox (IC50 = 10.67 μM), all the imido-naphthoquinone analogs (

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