dimethyldioxirane

Reputable manufacturer supply dimethyldioxirane 74087-85-7 in stock with high standard We provide high quality dimethyldioxirane (CAS 74087-85-7), at a very affordable prices to our customers.

1.What is the dimethyldioxirane ?

Dimethyldioxirane (DMDO) is a mild and selective oxidant widely used in organic synthesis for reactions such as oxidative cleavage, epoxidation, and functional group transformations. It efficiently converts cyanoketophosphoranes into α-keto esters and amides under mild conditions and is employed in stereoselective epoxidations, including glucal epoxide formation. DMDO is also useful for generating medium-ring keto-lactones via oxidative cleavage of bicyclic precursors. Its reactivity can be tuned by structural modifications, as seen in the chemoselective oxidation of lactams, where electronic properties influence the preference for N-H or C-H oxidation. The oxidant is valued for its compatibility with sensitive substrates and functional groups, making it a versatile tool in synthetic chemistry.

Dimethyldioxirane acts as a valuable oxidant for the synthesis of polyfunctional aromatic imidazolium monomers bearing epoxides.

2.What is the CAS number for dimethyldioxirane ?

The CAS number of dimethyldioxirane is 74087-85-7.

More information of dimethyldioxirane 74087-85-7 are:

3.What is the molecular formula of dimethyldioxirane ?

The chemical formula of?dimethyldioxirane is C3H6 O2 which containing 3 Carbon atoms,6 Hydrogen atoms and 2 Oxygen atoms,and the molecular weight, and the molecular weight of dimethyldioxirane is 74.0794

4.What is dimethyldioxirane(74087-85-7)used for?

Dimethyldioxirane (DMDO) is a mild and selective oxidant widely used in organic synthesis for reactions such as oxidative cleavage, epoxidation, and functional group transformations. It efficiently converts cyanoketophosphoranes into α-keto esters and amides under mild conditions and is employed in stereoselective epoxidations, including glucal epoxide formation. DMDO is also useful for generating medium-ring keto-lactones via oxidative cleavage of bicyclic precursors. Its reactivity can be tuned by structural modifications, as seen in the chemoselective oxidation of lactams, where electronic properties influence the preference for N-H or C-H oxidation. The oxidant is valued for its compatibility with sensitive substrates and functional groups, making it a versatile tool in synthetic chemistry.

InChI:InChI=1/C3H6O2/c1-3(2)4-5-3/h1-2H3

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5.Reputable manufacturer supply dimethyldioxirane 74087-85-7 in stock with high standard

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