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  2. Pyrrole - Wikipedia

    en.wikipedia.org/wiki/Pyrrole

    Pyrrole has a nutty odor. Pyrrole is a 5-membered aromatic heterocycle, like furan and thiophene. Unlike furan and thiophene, it has a dipole in which the positive end lies on the side of the heteroatom, with a dipole moment of 1.58 D. In CDCl 3, it has chemical shifts at 6.68 (H2, H5) and 6.22 (H3, H4).

  3. Paal–Knorr synthesis - Wikipedia

    en.wikipedia.org/wiki/Paal–Knorr_synthesis

    Pyrrole Ring. The Paal–Knorr reaction is quite versatile. In all syntheses almost all dicarbonyls can be converted to their corresponding heterocycle. R2 and R5 can be H, aryl or alkyl. R3 and R4 can be H, aryl, alkyl, or an ester. In the pyrrole synthesis (X = N), R1 can be H, aryl, alkyl, amino, or hydroxyl. [9]

  4. Knorr pyrrole synthesis - Wikipedia

    en.wikipedia.org/wiki/Knorr_pyrrole_synthesis

    The Knorr pyrrole synthesis is a widely used chemical reaction that synthesizes substituted pyrroles (3). [ 1 ] [ 2 ] [ 3 ] The method involves the reaction of an α- amino - ketone (1) and a compound containing an electron-withdrawing group (e.g. an ester as shown) α to a carbonyl group (2) .

  5. Hantzsch pyrrole synthesis - Wikipedia

    en.wikipedia.org/wiki/Hantzsch_pyrrole_synthesis

    [1] [2] Pyrroles are found in a variety of natural products with biological activity, so the synthesis of substituted pyrroles has important applications in medicinal chemistry. [3] [4] Alternative methods for synthesizing pyrroles exist, such as the Knorr Pyrrole Synthesis and Paal-Knorr Synthesis. The Hantzsch pyrrole synthesis

  6. Polypyrrole - Wikipedia

    en.wikipedia.org/wiki/Polypyrrole

    Polypyrrole Pyrrole can be polymerised electrochemically. [1] Polypyrrole (PPy) is an organic polymer obtained by oxidative polymerization of pyrrole. It is a solid with the formula H(C 4 H 2 NH) n H. It is an intrinsically conducting polymer, used in electronics, optical, biological and medical fields. [2] [3]

  7. Ehrlich's reagent - Wikipedia

    en.wikipedia.org/wiki/Ehrlich's_reagent

    It gives a negative test-result for 25I-NBOMe and many other non-indole-related psychoactives. The reagent will also give a positive result for opium, because of the presence of tryptophan in natural opium. [3] Pyridoxine, present in vitamin supplements, can give positive results to the Ehrlich test, showing a pink colour change. [4]

  8. What Really Causes a False Positive COVID-19 Test? Experts ...

    www.aol.com/false-positive-covid-19-test...

    False positive COVID-19 tests—when your result is positive, but you aren’t actually infected with the SARS-CoV-2 virus—are a real, if unlikely, possibility, especially if you don’t perform ...

  9. Indoleamine 2,3-dioxygenase - Wikipedia

    en.wikipedia.org/wiki/Indoleamine_2,3-dioxygenase

    Indoleamine-pyrrole 2,3-dioxygenase (IDO or INDO EC 1.13.11.52) is a heme-containing enzyme physiologically expressed in a number of tissues and cells, such as the small intestine, lungs, female genital tract or placenta. [5] In humans is encoded by the IDO1 gene. [6] IDO is involved in tryptophan metabolism.