3297-78-7

Upstream product

• 3297-75-4 3-hydroxy-1-phenyl-1,2,3,4-tetrahydroquinoline 
• 108-24-7 acetic anhydride 
• 122-39-4 diphenylamine 

Downstream Products

• 3297-75-4 3-hydroxy-1-phenyl-1,2,3,4-tetrahydroquinoline 
• 1529853-63-1 1-phenyl-3-propoxy-1,2,3,4-tetrahydroquinoline-6-carbaldehyde-N-4-(3-carboxymethyl-4-oxo-2-thioxo-1,3-thiazolidin-5-ylidenmethyl)phenyl-N-phenylhydrazone 
• 1564287-81-5 2-{4-oxo-5-[4-(1-phenyl-2-(3-nonyloxy-1-phenyl-1,2,3,4-tetrahydroquinolin-6-methy-lene)hydrazinyl)benzylidene]-2-thioxothiazolidin-3-yl}acetic acid 
• 1564287-82-6 2-cyano-3-{4-[1-phenyl-2-(1-phenyl-3-propoxy-1,2,3,4-tetrahydroquinolin-6-methy-lene)hydrazinyl]phenyl}acrylic acid 
• 1175004-74-6 1-phenyl-3-propoxy-1,2,3,4-tetrahydroquinoline-6-carbaldehyde 
• 1564287-76-8 3-nonyloxy-1-phenyl-1,2,3,4-tetrahydroquinoline-6-carbaldehyde 
• 1529853-61-9 1-phenyl-3-propoxy-1,2,3,4-tetrahydroquinoline-6-carbaldehyde N-phenylhydrazone 
• 1564287-77-9 3-nonyloxy1-phenyl-1,2,3,4-tetrahydroquinoline-6-carbaldehyde N-phenylhydrazone 
• 1529853-62-0 1-phenyl-3-propoxy-1,2,3,4-tetrahydroquinoline-6-carbaldehyde-N-(4-formyl)phenyl-N-phenyl-hydrazone 
• 1564287-78-0 3-nonyloxy-1-phenyl-1,2,3,4-tetrahydroquinoline-6-carbaldehyde N-(4-formyl)phenyl-N-phenylhydrazone 
• 1564287-79-1 2-[5-(3-hydroxy-1-phenyl-1,2,3,4-tetrahydroquinolin-6-methylene)-4-oxo-2-thioxothia-zolidin-3-yl]acetic acid 
• 1564287-80-4 2-[4-oxo-5-(1-phenyl-3-propoxy-1,2,3,4-tetrahydroquinolin-6-methylene)-2-thioxo-thiazolidin-3-yl]acetic acid 
• 1330779-12-8 1,2-bis(3-oxiranylmethoxy-1-phenyl-1,2,3,4-tetrahydroquinoline-6-ylmethylene)azine 
• 1330779-11-7 1,2-bis(3-hydroxy-1-phenyl-1,2,3,4-tetrahydroquinoline-6-ylmethylene)azine 

Relevant academic research and scientific papers

Hydrazones possessing a phenyl-1,2,3,4-tetrahydroquinoline moiety as hole transporting materials

Hydrazones containing 1-phenyl-1,2,3,4-tetrahydroquinoline units were synthesized starting from diphenylamine. These compounds were found to constitute novel hole transporting materials and were characterized by the time of flight method. The hole drift m

Copper(II)-catalyzed aminooxygenation and carboamination of N-aryl-2-allylanilines

The scope of the intramolecular copper(II)-catalyzed carboamination and aminooxygenation reactions of olefins has been extended to include N-aryl-2-allylanilines. These substrates exhibit divergent reactivity under catalytic vs. stoichiometric conditions.