90141-86-9

Upstream product

• 103529-16-4 2-[(trimethylsilyl)ethynyl]aniline 
• 187463-09-8 (Z)-1-(2-bromovinyl)-2-chlorobenzene 
• 24009-93-6 diethyl dihydrocinnoline-1,2-dicarboxylate 
• 1393462-68-4 C₁₄H₁₅ClN₂O₄ 
• 1393462-70-8 diethyl 4-(4-methoxyphenyl)dihydrocinnoline-1,2-dicarboxylate 
• 94026-82-1 1-(2-aminophenyl)-1’-(4-methoxyphenyl)ethan-1-ol 
• 875-66-1 cinnolin-4-ol 
• 615-43-0 2-iodophenylamine 
• 5152-84-1 4-chlorocinnoline 
• 5720-07-0 4-methoxyphenylboronic acid 

Downstream Products

• 108949-95-7 4-cinnolin-4-yl-phenol 
• 5782-23-0 3-(4-methoxy-phenyl)-1H-indole 
• 100382-29-4 5-(4-methoxy-phenyl)-pyridazine-3,4-dicarboxylic acid 
• 297134-04-4 8-iodo-4-(4'-methoxyphenyl)-3-trimethylsilylcinnoline 
• 297134-10-2 4-(4'-methoxyphenyl)-8-(3'-nitrophenyl)-3-trimethylsilylcinnoline 
• 297134-08-8 4-(4'-methoxyphenyl)-8-(4'-trifluoromethylphenyl)-3-trimethylsilylcinnoline 
• 297134-02-2 4-(4'-methoxyphenyl)-3-trimethylsilylcinnoline 

Relevant academic research and scientific papers

Copper-catalyzed tandem C-N bond formation: An efficient annulative synthesis of functionalized cinnolines

Cinn-tillating synthesis: The combination of a readily available copper catalyst, a simple hydrazide nucleophile, and established difunctionalized building blocks provides a new, flexible route to an under-developed class of aromatic heterocycles, cinnolines (see scheme). Copyright

Synthesis of 4,8-diarylcinnolines and quinazolines with potential applications in nonlinear optics. Diazines. Part 28

New 4,8-diarylbenzodiazines have been synthesized using cross-coupling reactions and regioselective metalation at the peri-position C8 of the benzene moiety of various cinnolines and quinazolines. Some of these compounds have been tested to assess their nonlinear optical properties. (C) 2000 Elsevier Science Ltd.