18979-90-3

Upstream product

• 1450-74-4 5-chloro-2-hydroxyacetophenone 
• 64-17-5 ethanol 
• 106-48-9 4-chloro-phenol 
• 90-00-6 o-Hydroxyethylbenzene 
• 7647-01-0 hydrogenchloride 
• 75-03-6 ethyl iodide 
• 6342-64-9 2-methoxy-5-chloroacetophenone 
• 1216072-89-7 1-(5-chloro-2-methoxyphenyl)-1-ethanol 
• 56911-73-0 4-chloro-2-ethyl-1-methoxybenzene 
• 925-90-6 ethylmagnesium bromide 
• 120-83-2 2,4-dichlorophenol 
• 876-27-7 4-chlorophenyl acetate 

Downstream Products

• 6964-28-9 (2-ethyl-4-chloro-phenoxy)-acetic acid 
• 53347-18-5 Buttersaeure-<4-chlor-2-aethyl-phenylester> 
• 53346-74-0 5-Chlor-2-hydroxy-3-aethylbenzylalkohol 
• 53347-25-4 Pentansaeure-<4-chlor-2-aethyl-phenylester> 
• 53347-26-5 Hexansaeure-<4-chlor-2-aethyl-phenylester> 
• 53346-88-6 4-Chlor-2-aethyl-6-(4-fluor-3-aethyl)-benzylphenol 
• 53346-82-0 4-Chlor-2-aethyl-6-cyclopentylphenol 
• 53346-83-1 4-Chlor-2-aethyl-6-cyclohexylphenol 
• 53346-89-7 4-Chlor-2-aethyl-6-(4-methoxy-3-aethyl)benzylphenol 
• 53347-03-8 4-chloro-2-ethyl-6-nitrophenol 
• 53347-16-3 acetic acid-(2-ethyl-4-chloro-phenyl ester) 
• 53346-86-4 4-Chlor-2-aethyl-6-(3,4-dichlor)-benzylphenol 
• 29848-96-2 4-Chloro-2-ethyl-6-benzylphenol 
• 53346-96-6 4-Chlor-2-(β-hydroxyaethylamino)methyl-6-aethylphenol 

Relevant academic research and scientific papers

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

Chemical Compounds

The invention relates to sulfonamide derivatives, to their use in medicine, to compositions containing them, to processes for their preparation and to intermediates used in such processes. More particularly the invention relates to a new sulfonamide Nav1.7 inhibitors of formula (I): or a pharmaceutically acceptable salt thereof, wherein Ar1, X, R1, R2, R3, R4 and R5 are as defined in the description. Nav 1.7 inhibitors are potentially useful in the treatment of a wide range of disorders, particularly pain.

PROCESS FOR SELECTIVELY POLYMERIZING ETHYLENE AND CATALYST THEREFOR

The present invention generally relates to a process that selectively polymerizes ethylene in the presence of an alpha-olefin, and to a metal-ligand complex (precatalyst) and catalyst useful in such processes, and to related compositions. The present invention also generally relates to ligands and intermediates useful for preparing the metal-ligand complex and to processes of their preparation.

High ortho preference in Ni-catalyzed cross-coupling of halophenols with alkyl Grignard reagents

(Chemical Equation Presented) High preference of substitution at the position ortho to the hydroxy group was observed for Ni-catalyzed cross-coupling reactions of dihalophenols with alkyl Grignard reagents. Reactions of 2,4-dihalophenols, with various com

Ionic liquids as reagent and reaction medium: Preparation of alkyl aryl ethers

Room temperature ionic liquid, [bmIm]OH, is used as a green recyclable reaction medium and reagent for the alkylation of phenols in excellent yields. The recovered ionic liquid was reused five to six times with consistent activity.