15288-02-5

Basic information

• Product Name: 6-hydroxy-7-methoxy-3,4-dihydronaphthalen-1(2H)-one
• CAS NO: 15288-02-5
• Molecular Formula: C₁₁H₁₂O₃
• Molecular Weight: 192.2112
• Mol File: 15288-02-5.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 393°C at 760 mmHg
• Flash Point: 159.4°C
• Density: 1.238g/cm³
• Vapor Pressure: 9.72E-07mmHg at 25°C
• Refractive Index: 1.581
• CAS DataBase Reference: 6-hydroxy-7-methoxy-3,4-dihydronaphthalen-1(2H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: 6-hydroxy-7-methoxy-3,4-dihydronaphthalen-1(2H)-one(15288-02-5)
• EPA Substance Registry System: 6-hydroxy-7-methoxy-3,4-dihydronaphthalen-1(2H)-one(15288-02-5)

Safety Data

• Hazardous Substances Data: 15288-02-5(Hazardous Substances Data)

Upstream product

• 13575-75-2 6,7-dimethoxy-1-oxo-1,2,3,4-tetrahydronaphthalene 
• 3579-88-2 6-hydroxy-7-methoxy-1,2,3,4-tetrahydronaphthalene 
• 84-58-2 2,3-dicyano-5,6-dichloro-p-benzoquinone 
• 98799-44-1 trans 4-(3-hydroxy-4-methoxyphenyl)but-3-enoic acid 
• 98799-43-0 trans-4-(3,4-dimethoxyphenyl)but-3-enoic acid 
• 120-14-9 3,4-dimethoxy-benzaldehyde 
• 13575-74-1 4-(3,4-dimethoxyphenyl)butanoic acid 
• 621-59-0 isovanillin 
• 57596-01-7 4-(3-hydroxy-4-methoxyphenyl)butanoic acid 

Downstream Products

• 98799-68-9 2-(6-Isopropoxy-7-methoxy-1-oxo-1,2,3,4-tetrahydro-naphthalen-2-yl)-3,4,5-trimethoxy-benzoic acid 
• 52259-72-0 norfagaronine 

Relevant articles and documents

Formation and composition of new optically active compounds

The present invention is directed to tetrahydronaphthalene derivatives of α-conindendrin, β-conindendrin, sikkimotoxin, and podophyllotoxin having at least one methyleneoxy bridge wherein the oxygen atom extends to the benzhydrylic carbon atom.

Direct Synthesis of Benzophenanthridines and Benzophenanthridones via SRN1 Reactions

A straightforward and high-yield route to the 11,12-dihydrobenzophenanthridine (3) and 11,12-dihydrobenzophenanthridone (14) ring systems is based upon an SRN1 reaction between 2-halobenzylamines 1 or 2-halobenzoic acids 11 and enolates derived from tetralones 2.The efficient dehydrogenation of 3 or 14 gives the benzophenthridines 4 or benzophenanthridones 15.Use of properly substituted reactants leads to nitidine, avicine, and fagaronine and to analogues of those natural products.