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4-nitro-10-methyl-9-acridanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

83413-85-8

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83413-85-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83413-85-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,4,1 and 3 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 83413-85:
(7*8)+(6*3)+(5*4)+(4*1)+(3*3)+(2*8)+(1*5)=128
128 % 10 = 8
So 83413-85-8 is a valid CAS Registry Number.

83413-85-8Downstream Products

83413-85-8Relevant academic research and scientific papers

Fluorescent nitric oxide donor for the detection and killing of: Pseudomonas aeruginosa

Hibbard, Hailey A. J.,Reynolds, Melissa M.

, p. 2009 - 2018 (2019)

The epidemic of multidrug-resistant bacteria calls for the improvement of both detection methods for bacterial infections and methods of treatment. Nitric oxide is a known potent antibacterial agent, but due to its gaseous and highly reactive nature, it is difficult to incorporate into a stable antibacterial compound. In this paper, we synthesize a nitric oxide donor attached to a fluorescent compound, creating a material that can both detect and kill the deadly multi-drug resistant bacteria strain Pseudomonas aeruginosa. Detection occurs through a bacterial enzyme-activated color change, showing a clear and obvious change from blue to yellow under UV light. The synthesized compound spontaneously releases 853 μmol of nitric oxide/g from a 10 mM initial concentration. Antibacterial efficacy studies after exposing Pseudomonas aeruginosa to a 10 mM dose of the synthesized compound show a 55-75% reduction in bacteria after 24 hours. This work is the first instance of a small molecule dual-function material that can both detect and kill bacteria.

Nitration of the Acetanilide-type Compounds

Daszkiewicz, Zdzislaw,Kyziol, Janusz B.

, p. 44 - 50 (2007/10/02)

Some aromatic compounds containing the imino group (NH) were nitrated in acetic acid or anhydride, and the ortho/para ratios were measured.N-Methyl derivatives of the aforementioned compounds are much less reactive when nitrated under comparable conditions and give significantly lower o/p ratios.These results along with the literature data support the hypothesis that the acetanilide-type compounds are nitrated via N-nitro intermediates.

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