88058-45-1

Basic information

• Product Name: 8-(benzyloxy)-3,4-dihydronaphthalen-1(2H)-one
• Synonyms: 8-(benzyloxy)-3,4-dihydronaphthalen-1(2H)-one
• CAS NO: 88058-45-1
• Molecular Formula: C₁₇H₁₆O₂
• Molecular Weight: 252.30774
• Mol File: 88058-45-1.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 8-(benzyloxy)-3,4-dihydronaphthalen-1(2H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: 8-(benzyloxy)-3,4-dihydronaphthalen-1(2H)-one(88058-45-1)
• EPA Substance Registry System: 8-(benzyloxy)-3,4-dihydronaphthalen-1(2H)-one(88058-45-1)

Safety Data

• Hazardous Substances Data: 88058-45-1(Hazardous Substances Data)

Upstream product

• 7695-47-8 8-hydroxy-1,2,3,4-tetrahydro-1-naphthalenone 
• 100-44-7 benzyl chloride 
• 100-39-0 benzyl bromide 

Downstream Products

• 32744-30-2 2-phenyl-4,5-dihydro-3H-naphtho<1,8-bc>furan 
• 133601-17-9 8-(1-hydroxy-1-phenylmethyl)-1,2,3,4-tetrahydro-1-naphthalenone 
• 92422-33-8 8-Benzyloxy-3,4-dihydro-[1,2]naphthoquinone 2-oxime 
• 328097-25-2 10-Phenylmethoxy-5,6-dihydrobenzo[h]cinnolin-3(2H)-one 
• 92421-89-1 N-((1S,2S)-8-Benzyloxy-1-hydroxy-1,2,3,4-tetrahydro-naphthalen-2-yl)-acetamide 
• 92421-82-4 N-(8-Benzyloxy-1-oxo-1,2,3,4-tetrahydro-naphthalen-2-yl)-acetamide 
• 92421-98-2 (4aS,10bS)-10-Benzyloxy-4-ethyl-4a,5,6,10b-tetrahydro-4H-naphtho[1,2-b][1,4]oxazin-3-one 
• 162180-26-9 8'-benzyloxy-3'4'-dihydro-spiro[cyclopentane-1,2'(1'H)-naphthalen]-1'-one 

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.