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4-Nitro-N-{3-[(4-nitrobenzoyl)amino]phenyl}benzamide is a complex organic compound with the molecular formula C20H14N4O6. It is characterized by the presence of nitro groups (-NO2), amide (-CO-NH2), and benzene rings. 4-Nitro-N-{3-[(4-nitrobenzoyl)aMino]phenyl}benzaMide is a derivative of benzamide, with a 4-nitrobenzoyl group attached to the amino group of a phenyl ring, which in turn is connected to another benzamide moiety. The compound is known for its potential applications in the field of pharmaceuticals and materials science, particularly in the synthesis of dyes and pigments. Its chemical structure and properties make it a subject of interest for researchers studying the effects of nitro and amide functional groups on molecular behavior and reactivity.

4142-06-7

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4142-06-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4142-06-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,4 and 2 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4142-06:
(6*4)+(5*1)+(4*4)+(3*2)+(2*0)+(1*6)=57
57 % 10 = 7
So 4142-06-7 is a valid CAS Registry Number.

4142-06-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name bis-1,3-(4-nitrobenzamido)benzene

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

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More Details:4142-06-7 SDS

4142-06-7Relevant academic research and scientific papers

PRODRUGS FOR NITROREDUCTASE BASED CANCER THERAPY- 2: Novel amide/Ntr combinations targeting PC3 cancer cells

Güng?r, Tu?ba,?nder, Ferah C?mert,Tokay, Esra,Gülhan, ünzile Güven,Hac?o?lu, Nelin,Tok, Tu?ba Ta?k?n,?elik, Ayhan,K??kar, Feray,Ay, Mehmet

, p. 383 - 400 (2019/04/01)

The use of nitroreductases (NTR) that catalyze the reduction of nitro compounds by using NAD(P)H in GDEPT (Gene-directed enzyme prodrug therapy) studies which minimize toxicity at healthy cells and increases concentration of drugs at cancer cells is remarkable. Discovery of new prodrug/NTR combinations is necessary to be an alternative to known prodrug candidates such as CB1954, SN23862, PR-104A. For this aim, nitro containing aromatic amides (A1-A23) were designed, synthesized, performed in silico ADMET and molecular docking techniques in this study. Prodrug candidates were studied on reduction potentials with Ssap-NtrB by HPLC system. Also, cyototoxic properties and prodrug ability of these amides were investigated using different cancer cell lines such as Hep3B and PC3. As a result of theoretical and biological studies, combinations of A5, A6 and A20 with Ssap-NtrB can be suggested as potential prodrugs/enzyme combinations at NTR based cancer therapy compared with CB1954/NfsB.

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