85992-27-4

Usage

InChI:InChI=1/C13H6Cl2OS/c14-10-9-6-5-7-3-1-2-4-8(7)11(9)17-12(10)13(15)16/h1-6H

Upstream product

• 51557-26-7 3-(2-naphthyl)acrylic acid 
• 49711-14-0 (E)-3-(naphthalen-2-yl)acrylic acid 

Downstream Products

• 85992-28-5 3-Chloro-naphtho[1,2-b]thiophene-2-carboxylic acid 
• 96547-27-2 3-chloro-N-(3-methylphenyl)naphtho<1,2-b>thiophene-2-carboxamide 
• 96547-26-1 3-chloro-N-(2-methylphenyl)naphtho<1,2-b>thiophene-2-carboxamide 
• 85992-29-6 3-chloronaphtho<1,2-b>thiophene 
• 234-41-3 naphtho[1,2-b]thiophene 
• 268218-25-3 6-chloronaphtho[2',1':4,5]thieno[2,3-c]naphtho[1,2-f]quinoline 
• 96547-25-0 3-chloro-N-phenylnaphtho<1,2-b>thiophene-2-carboxamide 
• 96547-28-3 3-chloro-N-(4-methylphenyl)naphtho<1,2-b>thiophene-2-carboxamide 

Relevant academic research and scientific papers

Synthesis of the Isomeric Monomethyl Derivatives of the Novel Naphthothienoquinoline Ring System

The synthesis of the novel naphthothienoquinoline (11) ring system and four of the isomeric monomethyl derivatives is described.

SYNTHESIS AND CHEMICAL TRANSFORMATIONS OF ISOMERIC NAPHTHOTHIOPHENES

A new method for the preparation of naphtho- and naphthothiophene structures by arylation of acrylic acid with α- and β-iodonaphthalene and subsequent oxidation of the resulting trans-naphthylacrylic acids with thionyl chloride in the presence of triethylbenzylammonium chloride is proposed.