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2-Chloro-3,5-dinitrophenyl acetic acid is a chemical compound with the molecular formula C8H5ClN2O6. It is a yellow crystalline solid that is soluble in water, ethanol, and ether. 2-chloro-3,5-dinitrophenyl acetic acid is primarily used as a synthetic intermediate in the production of various pharmaceuticals, agrochemicals, and other chemical products. It is also known for its potential use as a herbicide and a growth regulator. Due to its reactivity and the presence of functional groups such as the nitro group and the chloro group, it is important to handle 2-chloro-3,5-dinitrophenyl acetic acid with care, as it can be hazardous and may have toxic effects.

6093-32-9

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6093-32-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6093-32-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,9 and 3 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6093-32:
(6*6)+(5*0)+(4*9)+(3*3)+(2*3)+(1*2)=89
89 % 10 = 9
So 6093-32-9 is a valid CAS Registry Number.

6093-32-9Downstream Products

6093-32-9Relevant academic research and scientific papers

TRANSCRIPTION FACTOR MODULATING COMPOUNDS AND METHODS OF USE THEREOF

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Page/Page column 52-53, (2010/11/05)

Substituted benzoimidazole compounds useful as anti-infectives that decrease resistance, virulence, or growth of microbes are provided. Methods of using substituted benzimidazole compounds, in, e.g., reducing virulence and infectivity, inhibiting biofilms and treating bacterial infections, are also provided.

N-Hydroxybenzimidazole inhibitors of ExsA MAR transcription factor in Pseudomonas aeruginosa: In vitro anti-virulence activity and metabolic stability

Grier, Mark C.,Garrity-Ryan, Lynne K.,Bartlett, Victoria J.,Klausner, Kevin A.,Donovan, Peter J.,Dudley, Caroline,Alekshun, Michael N.,Ken Tanaka,Draper, Michael P.,Levy, Stuart B.,Kim, Oak K.

scheme or table, p. 3380 - 3383 (2010/08/06)

ExsA is a multiple adaptational response (MAR) transcription factor, regulating the expression of a virulence determinant, the type III secretion system (T3SS) in Pseudomonas aeruginosa. Non-cytotoxic, non-antibacterial N-hydroxybenzimidazoles were identified as effective inhibitors of ExsA-DNA binding, and their potential utility as anti-virulence agents for P. aeruginosa was demonstrated in a whole cell assay. Select N-hydroxybenzimidazole inhibitors were stable in an in vitro human liver microsomal assay.

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