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Ethanone,1-(2-amino-4-chloro-5-fluorophenyl)is a chemical compound with a molecular formula C10H8ClFNO and a molecular weight of 221.629 g/mol. It is a derivative of acetophenone, with a substituted amino group at the 2-position and a chloro and fluorine substituent at the 4 and 5 positions, respectively, on the phenyl ring.

937816-87-0

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937816-87-0 Usage

Uses

Used in Pharmaceutical Research and Drug Development:
Ethanone,1-(2-amino-4-chloro-5-fluorophenyl)is used as a building block for the development of new drugs, particularly in the synthesis of new pharmaceutical compounds. Its unique structure and properties make it a promising candidate for further study and evaluation in the pharmaceutical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 937816-87-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,7,8,1 and 6 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 937816-87:
(8*9)+(7*3)+(6*7)+(5*8)+(4*1)+(3*6)+(2*8)+(1*7)=220
220 % 10 = 0
So 937816-87-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H7ClFNO/c1-4(12)5-2-7(10)6(9)3-8(5)11/h2-3H,11H2,1H3

937816-87-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-Amino-4-chloro-5-fluorophenyl)ethanone

1.2 Other means of identification

Product number -
Other names Ethanone,1-(2-amino-4-chloro-5-fluorophenyl)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:937816-87-0 SDS

937816-87-0Relevant academic research and scientific papers

ERBB/BTK INHIBITORS

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Page/Page column 186-187; 219, (2019/08/26)

Disclosed are compounds inhibiting ErbBs (e. g., EGFR or Her 2), especially mutant forms of ErbBs, and BTK, pharmaceutically acceptable salts, hydrates, solvates or stereoisomers thereof and pharmaceutical compositions comprising the compounds. The compou

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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