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  1. Acetanilide | C8H9NO | CID 904 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety/hazards/toxicity information, supplier lists, and more.

  2. 17 sty 2014 · A series of conformationally restricted acetanilides were synthesized and evaluated as β3-adrenergic receptor agonists (β3-AR) for the treatment of overactive bladder (OAB).

  3. 20 mar 2012 · The vaporization and fusion enthalpies of acetanilide and several of its derivatives have been measured and combined to provide their corresponding sublimation enthalpies. Since all of the materials examined are solid at T = 298.15 K, the vaporization enthalpies measured by correlation gas chromatography at this temperature are for the ...

  4. 15 sty 2018 · In this work a solid-liquid equilibrium model was applied to predict the solubility of acetanilide and its derivatives in water. The model requires fusion enthalpy, fusion temperature, and activity coefficients of the acetanilides. The latter were predicted in the considered acetanilide + water mixtures with PC-SAFT.

  5. 18 cze 2013 · Solubilities of three primary amides, namely, acetanilide, propanamide, and butanamide, in supercritical carbon dioxide were measured at T = (308.2, 313.2, and 323.2) K over the pressure range (9.0 to 40.0) MPa by a flow type apparatus.

  6. 17 mar 2017 · Here, we have used chemoproteomic platforms to map proteome-wide cysteine reactivity of acetochlor (AC), the most widely used acetanilide herbicide, in vivo in mice. We show that AC directly reacts with >20 protein targets in vivo in mouse liver, including the catalytic cysteines of several thiolase enzymes involved in mitochondrial and ...

  7. 1 maj 2015 · The acetamide group enables regioselective oxidative ortho-C-H activation reactions, such as Pd-catalyzed acylation. The synthetic utility of these transformations can be significantly enhanced by using the acetamide as a quasi-leaving group in a subsequent conventional Pd-catalyzed coupling or cross-coupling reaction.

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