1192-31-0

Usage

Uses

Used in Chemical Synthesis:
2,3-Epoxy-4-methylpentane is used as a reactive intermediate for various chemical synthesis processes due to its strained epoxy ring, which facilitates reactions with other compounds.
Used in Industrial Applications:
In the industrial sector, 2,3-Epoxy-4-methylpentane is utilized as a component in the production of various chemical products, taking advantage of its reactivity and properties to achieve desired outcomes in manufacturing processes.
Used in Research and Development:
2,3-Epoxy-4-methylpentane serves as a valuable compound in research and development settings, where its unique reactivity and properties are explored for potential applications in new chemical reactions and innovative synthesis methods.

Upstream product

• 2402-98-4 2-cyanopyridine N-oxide 
• 691-38-3 (Z)-4-methyl-2-pentene 
• 536-80-1 iodosylbenzene 

Downstream Products

• 97206-72-9 3-hydroxy-4-methyl-2-(phenylamino)pentane 
• 97206-72-9 3-hydroxy-4-methyl-2-(phenylamino)pentane 

Relevant academic research and scientific papers

Selective alkene oxidation with H2O2 and a heterogenized Mn catalyst: Epoxidation and a new entry to vicinal cis-diols

Covalent anchoring of 1,4-dimethyl-1,4,7-triazacyclononane on silica gel is the first step in the preparation of a heterogenized Mn catalyst. When H2O2 is used as the oxidant, this material can catalyze the vicinal cis- dihydroxylation of disubstituted olefins, as shown schematically here. Both enantiomers of the product are obtained.

Hydrocarbon oxidation with iodosylbenzene catalysed by the sterically hindered iron(III) 5-(pentafluorophenyl)-10,15,20-tris(2,6-dichlorophenyl)porphyrin in homogeneous solution and covalently bound to silica

Iron(III) 5-(pentafluorophenyl)-10,15,20-tris(2,6-dichlorophenyl)porphyrin has been synthesised and used to catalyse hydrocarbon oxidation by iodosylbenzene. In homogeneous solution it is shown to be a stable and effective catalyst for alkene epoxidation and alkane hydroxyladon with a selectivity and reactivity closer to iron(III)tetrakis(pentafluorophenyl)porphyrin than to iron(III) tetrakis(2,6-dichlorophenyl)porphyrin. The new sterically hindered iron porphyrin has also been covalently bound, by nucleophilic aromatic substitution to aminopropylated silica. The resulting heterogenised catalyst is also stable towards oxidation but is less reactive than its homogeneous analogue.

Photoinduced Nitrene, Carbene, and Atomic Oxygen Transfer Reactions Starting from the Corresponding Pyridinium N-, C-, and O-Ylides

Ultraviolet irradiation of the pyridinium ylides 1, 2, and 3 led to fragmentation of the exocyclic polar bonds, as well as to skeletal rearrangements.The photoinduced fragmentation processes gave the corresponding pyridines and highly reactive intermediates, i. e. ethoxycarbonylnitrene, dicyanocarbene and atomic oxygen (oxene), respectively.Trapping of the reactive intermediates by alkanes and alkenes permitted the determination of their spin multiplicity.Ethoxycarbonylnitrene was in its triplet ground state at the moment of its formation.Dicyanocarbene occurred as a mixture of singlet and triplet, as determined by dilution experiments with variable amounts of alkenes.As to atomic oxygen, all collected data point to its formation in solution in its triplet ground state.