90401-62-0

Upstream product

• 90401-67-5 4-(2-biphenylyl)butyric acid 
• 68449-30-9 5-bromo-1-tetralone 
• 98-80-6 phenylboronic acid 
• 123206-83-7 4-(2-Bromophenyl)-1-butanol 
• 90841-47-7 4-(2-bromophenyl)butanoic acid 
• 92013-30-4 4-(o-bromophenyl)butyryl chloride 
• 71813-50-8 1-bromo-2-(but-3-enyl)benzene 
• 3433-80-5 1-Bromo-2-bromomethyl-benzene 
• 90401-65-3 ethyl 4-(2-biphenylyl)-2-butenoate 
• 90401-66-4 ethyl 4-(2-biphenylyl)butyrate 

Downstream Products

• 910330-44-8 5-phenyl-1-tetralol 
• 90400-96-7 C₂₃H₂₁NO₃S 
• 910330-27-7 5-phenyl-3,4-dihydronaphthalen-2(1H)-one 
• 592549-18-3 8-phenyl-1,2-dihydronaphthalene 
• 90400-76-3 5-Phenyl-3,4-dihydro-2H-naphthalen-1-one oxime 

Relevant academic research and scientific papers

Novel ligands for the human histamine H1 receptor: Synthesis, pharmacology, and comparative molecular field analysis studies of 2-dimethylamino-5-(6)-phenyl-1,2,3,4-tetrahydronaphthalenes

This paper reports the synthesis of a novel series of (±)-2-dimethylamino- 5- and 6-phenyl-1,2,3,4-tetrahydronaphthalene derivatives (5- and 6-APTs), and, corresponding affinity, functional activity, and, molecular modeling studies with regard to drug des

Synthesis of 1-tetralone derivatives using a Stille cross coupling/friedel crafts acylation sequence

An efficient method of synthesis of 1-tetralones has been achieved featuring a Stille cross-coupling reaction as the key step.