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(2,4,5-trifluorophenoxy)acetic acid, also known as 2,4,5-TFA or 2,4,5-trichlorophenoxyacetic acid, is a synthetic chemical compound with the molecular formula C8H5Cl3O3. It is a derivative of phenoxyacetic acid, where three chlorine atoms are substituted for hydrogen atoms on the phenyl ring, and a trifluorophenoxy group is attached to the molecule. (2,4,5-trifluorophenoxy)acetic acid has been primarily used as a selective herbicide to control broadleaf weeds in various agricultural crops. However, due to its potential health and environmental risks, its production and use have been restricted or banned in many countries. The compound's chemical structure and properties make it persistent in the environment, and it has been linked to various adverse effects on human health and wildlife.

325-81-5

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325-81-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 325-81-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,2 and 5 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 325-81:
(5*3)+(4*2)+(3*5)+(2*8)+(1*1)=55
55 % 10 = 5
So 325-81-5 is a valid CAS Registry Number.

325-81-5Downstream Products

325-81-5Relevant academic research and scientific papers

Identification of anthranilic acid derivatives as a novel class of allosteric inhibitors of hepatitis C NS5B polymerase

Nittoli, Thomas,Curran, Kevin,Insaf, Shabana,DiGrandi, Martin,Orlowski, Mark,Chopra, Rajiv,Agarwal, Atul,Howe, Anita Y. M.,Prashad, Amar,Floyd, M. Brawner,Johnson, Bernard,Sutherland, Alan,Wheless, Karen,Feld, Boris,O'Connell, John,Mansour, Tarek S.,Bloom, Jonathan

, p. 2108 - 2116 (2008/02/06)

A series of potent anthranilic acid-based inhibitors of the hepatitis C NS5B polymerase has been identified. The inhibitors bind to a site on NS5B between the thumb and palm regions adjacent to the active site as determined by X-ray crystallography of the enzyme-inhibitor complex. Guided by both molecular modeling and traditional SAR, the enzyme activity of the initial hit was improved by approximately 100-fold, yielding a series of potent and selective NS5B inhibitors with IC50 values as low as 10 nM. These compounds were also inhibitors of the HCV replicon in cultured HUH7 cells.

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