27581-19-7

Upstream product

• 64-17-5 ethanol 
• 108-95-2 phenol 
• 6921-66-0 4-chloro-2-hydroxy acetophenone 

Downstream Products

• 81878-02-6 Nicotinic acid 2-acetyl-3-chloro-6-ethyl-phenyl ester 
• 81878-09-3 1-(6-Chloro-3-ethyl-2-hydroxy-phenyl)-3-pyridin-3-yl-propane-1,3-dione 
• 81877-83-0 (E)-1-(6-Chloro-3-ethyl-2-hydroxy-phenyl)-3-pyridin-3-yl-propenone 
• 81591-14-2 3'-ethyl-6'-chloro-2'-hydroxy-acetophenone 

Relevant academic research and scientific papers

Medical raw material 2-ethyl-5-chlorophenol synthesis method

The invention relates to a medical raw material 2-ethyl-5-chlorophenol synthesis method, wherein phenol is adopted as a raw material, and ethylation and a chlorine replacement reaction are performed at the PH value of 6-7 under 2 atmospheric pressures under the effects of solvents such as methanol and ethanol to obtain 2-ethyl-5-chlorophenol. According to the present invention, the medical raw material 2-ethyl-5-chlorophenol synthesis method is simple and efficient, is safe in operation, and is practical in the specific production.

AMINOALKYL PHENOL ETHER INHIBITORS OF INFLUENZA A VIRUS

The present invention is directed to the discovery of novel nonpeptidic small molecules that function as inhibitors of the influenza virus infection. In particular, the present invention is directed to the discovery of anti-influenza entry inhibitors with

Synthesis and antimicrobial activities of oxadiazoles, phthalazines and indolinones

A series of oxadiazoles 5 phthalizines 6-8, and indolinones 9,10 have been synthesized from 2-[oxyacetyl hydrazine]ethyl benzenes 3. The compounds are characterized and screened for their antimicrobial activities.