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Monoperoxysuccinic acid

This article uses the former nomenclature. Organoperoxysulfonic acids are named by inserting peroxy in the sulfonic acid name, eg, cyclohexaneperoxysulfonic acid [74232-61 ]. For diacids, the prefixes monoperoxy- or diperoxy- are used, eg, monoperoxysuccinic acid and diperoxyisophthahc acid [1786-87 ]. [Pg.118]

Oxidation. Succinic acid reacts with hydrogen peroxide, giving different products that depend on the experimental conditions peroxysuccinic acid [2279-96-1] (CH2COOOH)2, oxosuccinic acid [328-42-7] (oxaloacetic acid) malonic acid [141-82-2] or a mixture of acetaldehyde, malonic acid, and make acid [6915-15-7]. Succinic anhydride in dimethylformamide (DMF) with H2O2 gives monoperoxysuccinic acid [3504-13-0], HOOCCH2CH2COOOH, mp 107°C (70). [Pg.535]

Benzeneperoxyseleninic acid, 2337 Benzeneperoxy sulfonic acid, 2341 3-Chloroperoxybenzoic acid, 2676 Diperoxyazelaic acid, 3189 Diperoxyterephthalic acid, 2925 Monoperoxysuccinic acid, 1542 Peroxyacetic acid, 0837 Peroxybenzoic acid, 2733 3-Peroxycamphoric acid, 3348 Peroxycrotonic acid, 1535 Peroxyformic acid, 0420 Peroxyfuroic acid, 1837 Peroxyhexanoic acid, 2514 Peroxy propionic acid, 1236 Peroxytrifluoroacetic acid, 0666 Trichloroperoxyacetic acid, 0659 See 1 /-DI(BENZOYLPEROX Y)ARYLIODINES POLYMERIC PEROXYACIDS ORGANIC PEROXIDES... [Pg.334]

Monoperoxysuccinic acid, 1537 Monopotassium acetylide, 0667 Monopotassium perchlorylamide, 3988 Monorubidium acetylide, 0681 Monosilver acetylide, 0646 Monosodium acetylide, 0680 Monosodium cyanamide, 0381 4-Morpholinesulfenyl chloride, 1581 Morpholinium perchlorate, 1674... [Pg.2115]

Benzeneperoxyseleninic acid, 2330 Benzeneperoxysulfonic acid, 2334 3-Chloroperoxybenzoic acid, 2672 Diperoxyazelaic acid, 3183 Diperoxyterephthalic acid, 2920 Monoperoxysuccinic acid, 1537 Peroxyacetic acid, 0833 Peroxybenzoic acid, 2729 3-Peroxycamphoric acid, 3342 Peroxycrotonic acid, 1530 Peroxyformic acid, 0419 Peroxyfuroic acid, 1831 Peroxyhexanoic acid, 2508 Peroxypropionic acid, 1232 Peroxytrifluoroacetic acid, 0662 Trichloroperoxyacetic acid, 0655 POLYMERIC PEROXYACIDS See I,I-DI(BENZOYLPEROXY)ARYLIODINES See also ORGANIC PEROXIDES... [Pg.2529]

Peroxyformic, peroxyacetic and po-oxytrifluoroacetic acids are most commonly used to bring about this t of oxidation, but 2-sulfoperoxytenzoic acid, monoperoxysuccinic acid s and disuccinoyl -oxide (which is converted to monoperoxysuccinic acid by hydrolysis), also oxidize alkenes to [Pg.446]

Monopalmitate sorbitan. See Sorbitan palmitate Monopentaerythritol. See Pentaerythritol Monoperoxysuccinic acid. See Succinic acid peroxide... [Pg.2736]

Monoamine derivatives of fatty acids, 320 Monoclinic chain packing, 323 Monoclonal theory of smooth muscle proliferation, 539 Monoene acids and esters, 3, 273 see also individual compounds Monogalactosyldiacylglycerol, 35,314,491, 492, 515, 516, 523,384 Monoglucosyldiacylglycerol, 35 Monolayers, 338-41, 356, 380 Monolaurin, 362-64 Monomeric acids, 174 Monomyristin, 340 Mono-olein, 328, 364,382,384 Monoperoxymaleic add, 460 Monoperoxyphthalic acid, 460 Monoperoxysuccinic acid, 460 Monophytanylglycerol, 27 Monostearin, 333 Montanic acid, 1 Monotropic polymorphism, 325 MONSAVON process, 241 Mormon cricket, 145 Morphine, 80 see also Poppy seed oil Mouse, 144 Mowrah butter, 72 MS-API, 434 MS applications, 436 Mwcor lipids, 152,153, 478... [Pg.567]

Monoperoxysuccinic acid frans-Glycols from ethylene derivatives s. 19,192... [Pg.68]

Monoperoxysuccinic acid allowed to react at room temp, with hexanoic anhydride in the presence of sulfuric acid j -carboxypropionyl hexanoyl peroxide. Y 90%. F. e. s. G. Schroeder and R. Lombard, Bl. 196A, 542. [Pg.431]

A new vitamin A synthesis has been described featuring an efficient dehydration step without double bond migration Olefins can be obtained from glycols with complete control of the position as well as the stereochemistry of the double bond. Together with Irans-hydroxylations this reaction constitutes a general and unambiguous method for the interconversion of ci5- and trans-olefins Monoperoxysuccinic acid has recently been recommended for the conversion of olefins into trans-glycols Also a convenient preparation of methyl ketones from terminal olefins has been reported... [Pg.299]

See other pages where Monoperoxysuccinic acid is mentioned: [Pg.118]    [Pg.525]    [Pg.73]    [Pg.600]    [Pg.525]    [Pg.413]    [Pg.525]    [Pg.2438]    [Pg.4244]    [Pg.236]    [Pg.312]   


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