Welcome to LookChem.com Sign In|Join Free
  • or
(2-acetyl-4-chloro-5-methylphenoxy)acetic acid is a complex organic compound with the molecular formula C11H11ClO4. It features a phenoxy group with a 2-acetyl, 4-chloro, and 5-methyl substitution pattern, attached to an acetic acid moiety. This chemical is known for its potential applications in pharmaceuticals and agrochemicals, particularly as a synthetic intermediate for the development of various drugs and pesticides. Its structure provides a unique set of properties that can be exploited in the design of new compounds with specific therapeutic or pesticidal effects.

1019-76-7

Post Buying Request

1019-76-7 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

1019-76-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1019-76-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,1 and 9 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1019-76:
(6*1)+(5*0)+(4*1)+(3*9)+(2*7)+(1*6)=57
57 % 10 = 7
So 1019-76-7 is a valid CAS Registry Number.

1019-76-7Downstream Products

1019-76-7Relevant 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.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 1019-76-7