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  2. Phenanthrene - Wikipedia

    en.wikipedia.org/wiki/Phenanthrene

    Phenanthrene is used to make dyes, plastics, pesticides, explosives, and drugs. It has also been used to make bile acids, cholesterol and steroids. [3] Phenanthrene occurs naturally and also is a man-made chemical. Commonly, humans are exposed to phenanthrene through inhalation of cigarette smoke, but there are many routes of exposure.

  3. Pyrene - Wikipedia

    en.wikipedia.org/wiki/Pyrene

    Pyrene is a polycyclic aromatic hydrocarbon (PAH) consisting of four fused benzene rings, resulting in a flat aromatic system. The chemical formula is C 16 H 10.This yellow-green solid is the smallest peri-fused PAH (one where the rings are fused through more than one face).

  4. Benzo(c)phenanthrene - Wikipedia

    en.wikipedia.org/wiki/Benzo(c)phenanthrene

    Benzo[c]phenanthrene is a polycyclic aromatic hydrocarbon with the chemical formula C 18 H 12. It is a white solid that is soluble in nonpolar organic solvents. It is a nonplanar molecule [1] [2] consisting of the fusion of four fused benzene rings. The compound is of mainly theoretical interest but it is environmentally occurring [3] and ...

  5. 1,10-Phenanthroline - Wikipedia

    en.wikipedia.org/wiki/1,10-Phenanthroline

    It is a white solid that is soluble in organic solvents. The 1,10 refer to the location of the nitrogen atoms that replace CH's in the hydrocarbon called phenanthrene. Abbreviated "phen", it is used as a ligand in coordination chemistry, forming strong complexes with most metal ions. [3] [4] It is often sold as the monohydrate.

  6. Morphinan - Wikipedia

    en.wikipedia.org/wiki/Morphinan

    Morphinan has a phenanthrene core structure with the A ring remaining aromatic and the B and C rings being saturated, and an additional nitrogen-containing, six-membered, saturated ring, the D ring, being attached to carbons 9 and 13 of the core, and with the nitrogen being at position 17 of the composite.

  7. Phenanthrenoid - Wikipedia

    en.wikipedia.org/wiki/Phenanthrenoid

    The structures are 2,5-dihydroxy-4,9,10-trimethoxyphenanthrene, 2,5-dihydroxy-4-methoxyphenanthrene and 2,5,9-trihydroxy-4-methoxy-9,10-dihydrophenanthrene. These molecules are named plicatol A, B and C. [9] Nudol is a phenanthrene from the orchids Eulophia nuda, Eria carinata and Eria stricta.

  8. Category:Phenanthrenes - Wikipedia

    en.wikipedia.org/wiki/Category:Phenanthrenes

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  9. Retene - Wikipedia

    en.wikipedia.org/wiki/Retene

    Retene, methyl isopropyl phenanthrene or 1-methyl-7-isopropyl phenanthrene, C 18 H 18, is a polycyclic aromatic hydrocarbon present in the coal tar fraction, boiling above 360 °C. It occurs naturally in the tars obtained by the distillation of resinous woods. It crystallizes in large plates, which melt at 98.5 °C and boil at 390 °C.