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(4-Chloro-2-methoxy-phenoxy)-acetyl chloride is a chemical compound with the molecular formula C9H8Cl2O3. It is a derivative of acetyl chloride, featuring a 4-chloro-2-methoxyphenoxy group attached to the acetyl moiety. (4-Chloro-2-methoxy-phenoxy)-acetyl chloride is characterized by its reactivity, particularly as an acylating agent in organic synthesis, where it can be used to introduce an acetyl group into various substrates. It is also known for its potential applications in the pharmaceutical industry, particularly in the synthesis of certain drugs and intermediates. Due to its reactivity and the presence of chlorine and methoxy groups, it is important to handle (4-Chloro-2-methoxy-phenoxy)-acetyl chloride with care, following appropriate safety protocols to minimize potential hazards.

7678-24-2

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7678-24-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7678-24-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,6,7 and 8 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7678-24:
(6*7)+(5*6)+(4*7)+(3*8)+(2*2)+(1*4)=132
132 % 10 = 2
So 7678-24-2 is a valid CAS Registry Number.

7678-24-2Downstream Products

7678-24-2Relevant 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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