60573-58-2

Basic information

• Product Name: 6-METHOXY-1,2-DIHYDRO-NAPHTHALENE
• Synonyms: 6-METHOXY-1,2-DIHYDRO-NAPHTHALENE
• CAS NO: 60573-58-2
• Molecular Formula: C₁₁H₁₂O
• Molecular Weight: 160.21238
• Mol File: 60573-58-2.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 6-METHOXY-1,2-DIHYDRO-NAPHTHALENE(CAS DataBase Reference)
• NIST Chemistry Reference: 6-METHOXY-1,2-DIHYDRO-NAPHTHALENE(60573-58-2)
• EPA Substance Registry System: 6-METHOXY-1,2-DIHYDRO-NAPHTHALENE(60573-58-2)

Safety Data

• Hazardous Substances Data: 60573-58-2(Hazardous Substances Data)

Usage

Synthesis Reference(s)

Tetrahedron Letters, 37, p. 1941, 1996 DOI: 10.1016/0040-4039(96)00309-7

Upstream product

• 1730-48-9 6-methoxy-1,2,3,4-tetrahydronaphthalene 

Downstream Products

• 93-04-9 2-Methoxynaphthalene 
• 63320-02-5 6-methoxy-1a,2,3,7b-tetrahydronaphtho[1,2-b]oxirene 
• 1262722-78-0 (1R,2S)-N-(p-nitrobenzenesulfonyl)amino-1,2,3,4-tetrahydro-7-methoxynaphthalen-1,2-imine 
• 1262722-71-3 (1R,2S)-N-(p-methylbenzenesulfonyl)amino-1,2,3,4-tetrahydro-7-methoxynaphthalen-1,2-imine 
• 214401-42-0 [7-(4-Cyano-benzyloxy)-1,2,3,4-tetrahydro-naphthalen-2-yl]-acetic acid ethyl ester 
• 214401-46-4 ethyl {7-[2-(4-cyanophenyl)ethyl]-1,2,3,4-tetrahydro-2-naphthalenyl}acetate 
• 214401-43-1 [7-(4-Cyano-benzyloxy)-naphthalen-2-yl]-acetic acid ethyl ester 
• 4133-34-0 7-methoxyl-2-tetralone 
• 2717-56-8 2-(2-carboxy-ethyl)-5-methoxy-benzoic acid 

Relevant articles and documents

Ruthenium-Catalyzed Dehydrogenation Through an Intermolecular Hydrogen Atom Transfer Mechanism

The direct dehydrogenation of alkanes is among the most efficient ways to access valuable alkene products. Although several catalysts have been designed to promote this transformation, they have unfortunately found limited applications in fine chemical synthesis. Here, we report a conceptually novel strategy for the catalytic, intermolecular dehydrogenation of alkanes using a ruthenium catalyst. The combination of a redox-active ligand and a sterically hindered aryl radical intermediate has unleashed this novel strategy. Importantly, mechanistic investigations have been performed to provide a conceptual framework for the further development of this new catalytic dehydrogenation system.