92799-73-0

Basic information

• Product Name: Hydroperoxide, 2,3-dihydro-1H-inden-1-yl
• CAS NO: 92799-73-0
• Molecular Formula: C9H10O2
• Molecular Weight: 150.177
• Mol File: 92799-73-0.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Hydroperoxide, 2,3-dihydro-1H-inden-1-yl(CAS DataBase Reference)
• NIST Chemistry Reference: Hydroperoxide, 2,3-dihydro-1H-inden-1-yl(92799-73-0)
• EPA Substance Registry System: Hydroperoxide, 2,3-dihydro-1H-inden-1-yl(92799-73-0)

Safety Data

• Hazardous Substances Data: 92799-73-0(Hazardous Substances Data)

Upstream product

• 95-13-6 1-indene 
• 496-11-7 INDANE 

Downstream Products

• 83-33-0 inden-1-one 
• 53580-62-4 3-(hydroxyphenyl)propionaldehyde 
• 6351-10-6 1-Indanol 
• 697-64-3 (R)-indan-1-ol 
• 25501-32-0 (S)-indanol 

Relevant articles and documents

Direct hydroperoxygenation of conjugated olefins catalyzed by cobalt(II) porphyrin

A novel and direct synthesis of hydroperoxy compounds from various types of conjugated olefins was established via cobalt(II) porphyrin-catalyzed hydroperoxygenation. The reaction of α,β,γ,δ-unsaturated carbonyl compounds, acrylic esters, α-substituted acrylic esters and styrene derivatives with molecular oxygen and triethylsilane in the presence of a catalytic amount of cobalt(II) porphyrin proceeded rapidly to give the corresponding hydroperoxygenated compounds in high or moderate yields.

A novel copper(II)-lanthanum(IIi) metal organic framework as a selective catalyst for the aerobic oxidation of benzylic hydrocarbons and cycloalkenes

The synthesis and structure of a novel heteronuclear CuII and LaIII metal organic framework (MOF) having pyridinedicarboxylic acid (CuLa-MOF) is reported. The obtained MOF with the formula {[Cu0.5La2(HPDC)(PDC)2(SO4)(H2O)2]H2O}n (PDC: 3,5-pyridinedicarboxylate) has a 3D non-porous lattice with a single type of octahedrally coordinated CuII and two distinct nonacoordinated LaIII ions, with sulphate being a linker between the CuII and LaIII centers. CuLa-MOF exhibits catalytic activity to promote the aerobic autooxidation of benzylic hydrocarbons and the aerobic oxidation of cycloalkenes. Compared with a homogenous catalyst, Cu(OAc)2, CuLa-MOF, as a heterogeneous catalyst, exhibits similar activity, but the solid is recyclable with some minor decrease in activity from the first to the second catalytic cycle; after which, a steady activity is observed, as determined by the coincidence of temporal evolution of the reaction upon reuse.

Solvent-free, heterogeneous photooxygenation of hydrocarbons by Hyflon membranes embedding a fluorous-tagged decatungstate

Hybrid fluoropolymeric membranes with 25% loading of the fluorous-tagged (RfN)4W10O32 effect the solvent-free photooxygenation of benzylic C-H bonds with up to 6100 TONs in 4 hours. The Royal Society of Chemistry 2006.