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Mercapto compounds

Williamson s lethod, more particularly lor hydroxy- and thloT (mercapto) compounds. The substance is treated either directly with sodium or (more usually) with a solution of sodium methoxide in methanol, to give the sodium derivative. The latter is then boiled with methvl iodide. [Pg.217]

Multifunctional Hydroxy, Mercapto, and Amino Compounds. These are used to cross-link halogenated polymers. Depending on the labihty of the halogen, the cross-linking agents can be capped to reduce reactivity or used in combination with accelerators to increase the rate of reaction. Benzoyl capping is common with hydroxy and mercapto compounds forming the carbamate by reaction with one equivalent of carbon dioxide is used with diamines. [Pg.225]

Alkylation of these mercapto compounds in alkaline solution gives only the S-methyl derivatives. Of the four isomeric A-methyl derivatives, the 4-thioquinazolines, (28) and (29), have been obtained from the corresponding oxo compounds with phosphorus pentasulfide but the corresponding 2-thio derivatives (30) and (31) are not known. However, derivatives of substance (31) with methyl replaced by... [Pg.274]

Substituted-4-hydroxy-6-methylpyrimidines are formylated in the 5-position when the 2-substituent (e.g. NH2, OH) is sufficiently electron releasing. The related 4-mercapto compounds gave only the ortho-thio-esters. ... [Pg.76]

Apparently no data are available for mercapto compounds with hetero atoms-1,2 or for 4-(or 5)-mercapto compounds with hetero atoms-1,3. From the data available, the tautomerism of potential... [Pg.60]

Then, as described in U.S. Patent 2,55416, the 2-acetylamido-5-mercapto-1,3,4-thiadiazole is converted to the sulfonyl chloride by passing chlorine gas into a cooled (5°-10°C) solution in 33% acetic acid (66 parts to 4 parts of mercapto compound) used as a reaction medium. Chlorine treatment is continued for two hours. The crude product can be dried and purified by recrystallization from ethylene chloride. The pure compound is a white crystalline solid, MP l94°C,with decomposition, when heated rapidly. The crude damp sulfonyl chloride is converted to the sulfonamide by addition to a large excess of liquid ammonia. The product is purified by recrystallization from water. The pure compound is a white, crystalline solid, MP 259°C, with decomposition. The yield of sulfonamide was 85% of theory based on mercapto compound. [Pg.16]

Bergstrom et al. [63] used HPLC for determination of penicillamine in body fluids. Proteins were precipitated from plasma and hemolyzed blood with trichloroacetic acid and metaphosphoric acid, respectively, and, after centrifugation, the supernatant solution was injected into the HPLC system via a 20-pL loop valve. Urine samples were directly injected after dilution with 0.4 M citric acid. Two columns (5 cm x 0.41 cm and 30 cm x 0.41 cm) packed with Zipax SCX (30 pm) were used as the guard and analytical columns, respectively. The mobile phase (2.5 mL/min) was deoxygenated 0.03 M citric acid-0.01 M Na2HP04 buffer, and use was made of an electrochemical detector equipped with a three-electrode thin-layer cell. The method was selective and sensitive for mercapto-compounds. Recoveries of penicillamine averaged 101% from plasma and 107% from urine, with coefficients of variation equal to 3.68 and 4.25%, respectively. The limits of detection for penicillamine were 0.5 pm and 3 pm in plasma and in urine, respectively. This method is selective and sensitive for sulfhydryl compounds. [Pg.146]

An example for stimulus generalization are responses of rats to stress-inducing odors. Laboratoiy rats of the Wistar strain respond to predator odors, specifically mercapto compounds in fox droppings, with stress reactions, for example avoidance behavior such as freezing and increased plasma corticosterone concentrations (Vemet-Mauiy et ah, 1984). The rats were trained to avoid water scented with a mercapto odorant that contained both a keto- and a sulfhydryl group (4-mercapto-4-methyl-2-pentanone). As the animals licked a waterspout, a mild electric shock was applied to their tongue. When different compounds were tested thereafter, the rats avoided compounds with similar... [Pg.111]

Types of compounds are arranged according to the following system hydrocarbons and basic heterocycles hydroxy compounds and their ethers mercapto compounds, sulfides, disulfides, sulfoxides and sulfones, sulfenic, sulfinic and sulfonic acids and their derivatives amines, hydroxylamines, hydrazines, hydrazo and azo compounds carbonyl compounds and their functional derivatives carboxylic acids and their functional derivatives and organometallics. In each chapter, halogen, nitroso, nitro, diazo and azido compounds follow the parent compounds as their substitution derivatives. More detail is indicated in the table of contents. In polyfunctional derivatives reduction of a particular function is mentioned in the place of the highest functionality. Reduction of acrylic acid, for example, is described in the chapter on acids rather than functionalized ethylene, and reduction of ethyl acetoacetate is discussed in the chapter on esters rather than in the chapter on ketones. [Pg.321]

Mercapto compounds, oxidation of, 7 242-243 Mercaptodicyanamides, reaction with hexafluoroacetone, 30 267... [Pg.174]

Analogous to MOT the yellow 7-mercapto compound proves to be the thioxo tautomer (59JOC779). In 5,7-dialkyl-2-amino-TPs any imino structure is excluded by IRand NMR spectra (71AP856,71T3247) aminoa-zaindolizines generally behave similarly (91H(32)329). [Pg.108]


See other pages where Mercapto compounds is mentioned: [Pg.413]    [Pg.280]    [Pg.458]    [Pg.224]    [Pg.95]    [Pg.136]    [Pg.31]    [Pg.41]    [Pg.102]    [Pg.265]    [Pg.160]    [Pg.161]    [Pg.231]    [Pg.61]    [Pg.16]    [Pg.161]    [Pg.47]    [Pg.310]    [Pg.83]    [Pg.194]    [Pg.1062]    [Pg.232]    [Pg.362]    [Pg.93]    [Pg.211]    [Pg.342]    [Pg.224]    [Pg.192]    [Pg.124]    [Pg.458]    [Pg.931]    [Pg.95]    [Pg.136]    [Pg.411]    [Pg.103]    [Pg.211]   
See also in sourсe #XX -- [ Pg.411 ]




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Compounds with Potential Mercapto Groups

Mercapto

Mercapto compounds tautomerism

Mercapto compounds, oxidation

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