4676-82-8

Basic information

• Product Name: 2-TETRAHYDROFURYL HYDROPEROXIDE
• Synonyms: Tetrahydrofuran-2-hydroperoxid;2-hydroperoxytetrahydrofuran;2-tetrahydrofuryl hydroperoxide;tetrahydrofuran-2-yl-hydroperoxide;2-hydroperoxotetrahydrofyran;Tetrahydrofuran-2-hydroperoxide
• CAS NO: 4676-82-8
• Molecular Formula: C4H8O3
• Molecular Weight: 104.106
• Mol File: 4676-82-8.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 135.22°C (rough estimate)
• Density: 1.1141 (rough estimate)
• Refractive Index: 1.4462 (estimate)
• CAS DataBase Reference: 2-TETRAHYDROFURYL HYDROPEROXIDE (CAS DataBase Reference)
• NIST Chemistry Reference: 2-TETRAHYDROFURYL HYDROPEROXIDE (4676-82-8)
• EPA Substance Registry System: 2-TETRAHYDROFURYL HYDROPEROXIDE (4676-82-8)

Safety Data

• Safety Statements: A powerful oxidizer. The first autooxidation product of tetrahydrofuran. Readily changes to a highly explosive polyalkylidene peroxide. When heated to decomposition it emits acrid smoke and irritating fumes.
• HazardClass: 3
• Hazardous Substances Data: 4676-82-8(Hazardous Substances Data)

Upstream product

• 864943-41-9 (Z)-2-(2-chlorophenyl)-3,4-diphenyldec-3-en-5-yn-2-ol 
• 109-99-9 tetrahydrofuran 
• 864943-35-1 (Z)-2,3,4,6-tetraphenylhex-3-en-5-yn-2-ol 

Downstream Products

• 5371-52-8 2-hydroxytetrahydrofuran 
• 16237-62-0 3-(tetrahydrofuran-2-yl)propanenitrile 
• 25714-71-0 4-hydroxybutyraldehyde 
• 96-48-0 4-butanolide 
• 5453-67-8 2,6-bis(methoxycarbonyl)pyridine 
• 69945-43-3 Pyridin-2,6-di(monothiocarbonsaeure)-di-S-methyl ester 
• 1191-99-7 2,3-dihydro-2H-furan 
• 110-63-4 Butane-1,4-diol 

Relevant articles and documents

Interaction between the peroxide adduct of binuclear iron(III) complex with (HPTP) anion and the sugar moiety of nucleosides

We have in this study obtained the experimental evidence to suggest that the peroxide adduct of binuclear iron(III) complex with H(HPTP) directly reacts with the sugar moiety of the DNA chain, to cleave it; H(HPTP) denotes N,N,N′,N′-tetrakis(2-pyridylmeth

Cleavage of a carbon-carbon triple bond via gold-catalyzed cascade cyclization/oxidative cleavage reactions of (2)-enynols with molecular oxygen

A highly efficient carbon-carbon triple bond cleavage reaction of (Z)-enynols was developed, which offered a new route to highly substituted butenolides. The methodology is realized by a tandem reaction using a single gold(I) catalyst, which could catalyze different reactions of cyclization/oxidative cleavage in the same vessel. Copyright