99050-43-8

Basic information

• Product Name: 8-Benzyloxy-6-methoxytetralone
• Synonyms: 8-Benzyloxy-6-methoxytetralone
• CAS NO: 99050-43-8
• Molecular Weight: 282.339
• Mol File: 99050-43-8.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 8-Benzyloxy-6-methoxytetralone(CAS DataBase Reference)
• NIST Chemistry Reference: 8-Benzyloxy-6-methoxytetralone(99050-43-8)
• EPA Substance Registry System: 8-Benzyloxy-6-methoxytetralone(99050-43-8)

Safety Data

• Hazardous Substances Data: 99050-43-8(Hazardous Substances Data)

Upstream product

• 1078-19-9 6-methoxy-3,4-dihydro-1(2H)-naphthalenone 
• 99050-38-1 4-(3,5-Dimethoxyphenyl)butyric acid methyl ester 
• 99050-36-9 3-(3,5-dimethoxyphenyl) propionic acid chloride 
• 100-39-0 benzyl bromide 
• 99050-42-7 8-hydroxy-6-methoxy-1-tetralone 
• 78-93-3 butanone 
• 99050-37-0 1-Diazo-4-(3,5-dimethoxy-phenyl)-butan-2-one 
• 717-94-2 3-(3,5-dimethoxyphenyl)propionic acid 
• 91555-31-6 4-(3,5-dimethoxyphenyl)butanoic acid 
• 883-07-8 6,8-dimethoxy-3,4-dihydro-2H-naphthalen-1-one 

Downstream Products

• 71135-80-3 cannithrene-1 
• 99050-49-4 5-Benzyloxy-7-methoxy-phenanthren-3-ol 
• 99050-48-3 5-Benzyloxy-7-methoxy-9,10-dihydro-phenanthren-3-ol 
• 99050-47-2 8-Benzyloxy-6-methoxy-2-(3-oxo-butyl)-3,4-dihydro-2H-naphthalen-1-one 
• 99050-46-1 5-Benzyloxy-7-methoxy-1,9,10,10a-tetrahydro-2H-phenanthren-3-one 
• 99050-45-0 8-Benzyloxy-6-methoxy-1-oxo-2-(3-oxo-butyl)-1,2,3,4-tetrahydro-naphthalene-2-carbaldehyde 
• 99050-44-9 3,4-Dihydro-2-(hydroxymethylene)-6-methoxy-8-(phenylmethoxy)-1(2H)-naphthalenone 

Relevant articles and documents

Enantioselective Ruthenium-Catalyzed Benzocyclobutenone-Ketol Cycloaddition: Merging C-C Bond Activation and Transfer Hydrogenative Coupling for Type II Polyketide Construction

The first enantioselective intermolecular metal-catalyzed cycloadditions of benzocyclobutenones via C-C bond oxidative addition are described. In the presence of a ruthenium(0) complex modified by (R)-DM-SEGPHOS, tetralone-derived ketols and benzocyclobutenones combine to form cycloadducts with complete regio- and diastereoselectivity and high enantioselectivity. Using this method, the "bay region" substructure of the angucycline natural product arenimycin was prepared.

Urokinase inhibitors

Compounds having the formula are inhibitors of urokinase and are useful in the treatment of diseases in which urokinase plays a role. Also disclosed are urokinase-inhibiting compositions and a method of inhibiting urokinase in a mammal.