68707-66-4

Upstream product

• 76635-76-2 2-(Hydroxymethyl)-1-methoxynaphthalene 
• 98-80-6 phenylboronic acid 
• 36441-32-4 2-benzyl-1-naphthol 
• 74-88-4 methyl iodide 

Downstream Products

• 123239-57-6 2-Benzyl-1-methoxy-4-methylsulfanyl-naphthalene 
• 109381-48-8 1-methoxy-2-benzyl-4-naphthoic acid 
• 109381-49-9 3-(Phenylmethyl)-4-hydroxy-1-naphthoic acid 
• 109381-54-6 4-Phenyl-2-(phenylmethyl)-1-naphthol 
• 109381-53-5 1-methoxy-2-benzyl-4-phenylnaphthalene 
• 123239-51-0 4-nitro-2-benzyl-1-naphthol 
• 123239-50-9 2-Benzyl-4-methanesulfonyl-naphthalen-1-ol 
• 109381-58-0 4-Aminosulfonyl-2-(phenylmethyl)-1-naphthol 
• 123239-58-7 1-metoxy-2-benzyl-4-(methylsulfonyl)naphthalene 
• 109381-44-4 1-methoxy-2-benzyl-4-bromonaphthalene 
• 109381-40-0 4-Bromo-2-(phenylmethyl)-1-naphthol 
• 68707-67-5 1-methoxy-2-benzyl-4-nitronaphthalene 

Relevant academic research and scientific papers

Nickel-Catalyzed Suzuki-Miyaura Cross-Coupling Reaction of Naphthyl and Quinolyl Alcohols with Boronic Acids

A nickel-catalyzed C(sp3)-C(sp2) Suzuki cross-coupling of arylboronic acids and (hetero)naphthyl alcohols has been developed. A Ni(dppp)Cl2 complex showed the highest efficiency and broadest substrate scope. High functiona

2-Substituted-1-naphthols as potent 5-lipoxygenase inhibitors with topical antiinflammatory activity

The synthesis, biological evaluation, and structure-activity relationships of a series of 1-naphthols bearing carbon substituents at the 2-position are described. These compounds are potent inhibitors of the 5-lipoxygenase from RBL-1 cells and also inhibi

2-substituted-1-naphthols, pharmaceutical compositions of, and their use as 5-lipoxygenase inhibitors

2-Substituted-1-naphthols are 5-lipoxygenase inhibitors which make them useful in the treatment of inflammation, obstructive lung diseases and/or psoriasis. Useful 2-substituent groups are alkyls, alkenyls, alkynyls, cycloalkyls, cycloalkenyls, the groups