5385-28-4

Basic information

• Product Name: indan-4-yl-phenyl ketone
• CAS NO: 5385-28-4
• Molecular Weight: 222.287
• Mol File: 5385-28-4.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: indan-4-yl-phenyl ketone(CAS DataBase Reference)
• NIST Chemistry Reference: indan-4-yl-phenyl ketone(5385-28-4)
• EPA Substance Registry System: indan-4-yl-phenyl ketone(5385-28-4)

Safety Data

• Hazardous Substances Data: 5385-28-4(Hazardous Substances Data)

Upstream product

• 77635-15-5 1-Indanol-7-carboxylic acid 
• 4044-54-6 2,3-dihydro-1H-indene-4-carboxylic acid 
• 65898-33-1 (2,3-dihydro-1H-inden-4-yl)methanol 
• 51932-70-8 indane-4-carboxaldehyde 
• 7603-37-4 2,3,4,7-tetrahydro-indene 
• 501-65-5 diphenyl acetylene 
• 6134-53-8 4-bromo-2,3-dihydro-1H-indene 
• 100-47-0 benzonitrile 

Downstream Products

• 641-48-5 aceanthrene 
• 201486-99-9 (+/-)-Hydroxy-phenyl-(indanyl-⁽⁴⁾)-methan 

Relevant articles and documents

Photochemically generated bicyclic ortho-quinodimethanes: Photo- enolization of bicyclic aldehydes and ketones

A photoenolization route to bicyclic ortho-quinodimethanes was investigated. Bicyclic photoenols were trapped in an intermolecular fashion with various dienophiles for the first time. All ortho-quinodimethane precursors were prepared via a selective route commencing with 1-indanol, α- tetralol and 1-benzosuberone. Irradiation afforded the E-photoenols exclusively which were trapped with equal efficiency except that derived from indane-4-carboxaldehyde. This low efficiency has been ascribed to rapid auto- oxidation of the aldehyde to carboxylic acid. The facial selectivity of the reaction between the photoenol from benzosuberan-9-carboxaldehyde and dimethyl fumarate was much lower when compared to the other aldehydes in this study. A distorted diene caused by the presence of the seven membered ring explains these results.