56541-64-1

Upstream product

• 56961-40-1 1,3,4-trichloro-[2]naphthol 
• 7732-18-5 water 
• 859776-19-5 2-chloro-3-methoxynaphthalene 
• 93-04-9 2-Methoxynaphthalene 
• 64-17-5 ethanol 
• 116632-06-5 1,3-dichloronaphthol 
• 7664-93-9 sulfuric acid 

Downstream Products

• 6357-85-3 2-naphthol-4-sulfonic acid 
• 1338475-04-9 3,3'-di chloro-[1,1'-binaphthalene]-2,2'-diol 
• 116-63-2 1-amino-2-naphthol-4-sulfonic acid 
• 6639-33-4 3-chloro-[1,2]naphthoquinone 1-oxime 

Relevant academic research and scientific papers

Asymmetric dearomatization of naphthols via a Rh-catalyzed C(sp2)-H functionalization/annulation reaction

A Rh-catalyzed enantioselective dearomatization of 1-aryl-2-naphthols with internal alkynes via C-H functionalization reaction was achieved. In the presence of a chiral Cp/Rh catalyst and combined oxidants of Cu(OAc)2 and air (oxygen), various

ION CHANNEL ANTAGONISTS/BLOCKERS AND USES THEREOF

Provided are ion channel antagonists/blockers and uses thereof. Specifically, it provides the compounds of formula (I) or pharmaceutically acceptable salts, stereoisomers, solvates or prodrugs, preparation method therefor and application thereof. Definition of each group in the formula can be found in the specification for details. Provided is also pharmaceutical composition useful for treatment of heart disease and other ion channel related diseases.