338989-86-9

Upstream product

• 338989-70-1 4-manisylpyridine 
• 19524-06-2 4-bromopyridine hydrochloride 
• 6267-34-1 2-bromo-5-methoxy-1,3-dimethyl-benzene 

Downstream Products

• 1056700-83-4 7-bromo-2-[4-(4-methoxy-2,6-dimethylphenyl)-pyridin-2-yl]-1,10-phenanthroline 
• 1056700-77-6 8-bromo-2-[4-(4-methoxy-2,6-dimethylphenyl)-pyridin-2-yl]-1,10-phenanthroline 
• 1056700-72-1 9-iodo-2-[4-(4-methoxy-2,6-dimethylphenyl)-pyridin-2-yl]-1,10-phenanthroline 

Relevant academic research and scientific papers

Synthesis of aryl-substituted 2-pyridyl-1,10-phenanthrolines; A series of oriented terpyridine analogues

A 3 × 3 matrix of manisyl (4-methoxy-2,6-dimethylphenyl) substituted pyridyl-1,10-phenanthrolines has been synthesized by utilizing a general palladium catalyzed cross-coupling procedure. The directionality of these terdentate ligands will generate chiral

Synthesis and fluorescence properties of manisyl-substituted terpyridine, bipyridine, and phenanthroline

As a hybrid of two aryl motifs, that is p-anisyl and mesityl, the 4-methoxy-2,6-dimethylphenyl or "manisyl" substituent offers possibilities for further structural elaboration as well as enhancing the solubility of the heterocyclic ligands mentioned in th