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2. List of water-miscible solvents - Wikipedia

   en.wikipedia.org/wiki/List_of_water-miscible...

   The following compounds are liquid at room temperature and are completely miscible with water; ... pyridine: 110-86-1 C 4 H 8 O 2 S: sulfolane: 126-33-0 (CH 2) 4 O ...

3. Oxidation with chromium(VI) complexes - Wikipedia

   en.wikipedia.org/wiki/Oxidation_with_chromium(VI...

   Cr(VI)-pyridine and pyridinium reagents have the advantage that they are soluble in organic solvents as are the alcohol substrates. One family of reagents employs the complex CrO 3 (pyridine) 2. [2] Sarett's reagent: a solution of CrO 3 (pyridine) 2 in pyridine. It was popularized for selective oxidation of primary and secondary alcohols to ...

4. Transition metal pyridine complexes - Wikipedia

   en.wikipedia.org/wiki/Transition_metal_pyridine...

   Transition metal pyridine complexes encompass many coordination complexes that contain pyridine as a ligand. Most examples are mixed-ligand complexes. Most examples are mixed-ligand complexes. Many variants of pyridine are also known to coordinate to metal ions, such as the methylpyridines, quinolines, and more complex rings.

5. The 12 Best Water Softeners of 2022 - AOL

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6. Pyridine - Wikipedia

   en.wikipedia.org/wiki/Pyridine

   Pyridine is a basic heterocyclic organic compound with the chemical formula C 5 H 5 N. It is structurally related to benzene, with one methine group (=CH−) replaced by a nitrogen atom (=N−). It is a highly flammable, weakly alkaline, water-miscible liquid with a distinctive, unpleasant fish

7. Pyridinium chlorochromate - Wikipedia

   en.wikipedia.org/wiki/Pyridinium_chlorochromate

   Pyridinium chlorochromate in a vial. Pyridinium chlorochromate (PCC) is a yellow-orange salt with the formula [C 5 H 5 NH] + [CrO 3 Cl] −.It is a reagent in organic synthesis used primarily for oxidation of alcohols to form carbonyls.