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  2. Neopentane - Wikipedia

    en.wikipedia.org/wiki/Neopentane

    Therefore, neopentane is a gas at room temperature and atmospheric pressure, while the other two isomers are (barely) liquids. The melting point of neopentane (−16.6 °C), on the other hand, is 140 degrees higher than that of isopentane (−159.9 °C) and 110 degrees higher than that of n -pentane (−129.8 °C).

  3. Jmol - Wikipedia

    en.wikipedia.org/wiki/Jmol

    JSmol is an implementation in JavaScript of the functionality of Jmol. [4] It can hence be embedded in web pages to display interactive 3D models of molecules and other structures without the need for any software apart from the web browser (it does not use Java).

  4. Neopentylamine - Wikipedia

    en.wikipedia.org/wiki/Neopentylamine

    5813-64-9 3D model . Interactive image; ChemSpider: 72173; ECHA InfoCard: ... The molecule is the primary amine derivative of neopentane, (CH 3) 4 C.

  5. Pentaerythritol tetranitrate - Wikipedia

    en.wikipedia.org/wiki/Pentaerythritol_tetranitrate

    Pentaerythritol tetranitrate (PETN), also known as PENT, pentyl, PENTA (ПЕНТА, primarily in Russian), TEN (tetraeritrit nitrate), corpent, or penthrite (or, rarely and primarily in German, as nitropenta), is an explosive material.

  6. p-Anisidine - Wikipedia

    en.wikipedia.org/wiki/P-Anisidine

    p-Anisidine condenses readily with aldehydes and ketones to form Schiff bases, which absorb at 350 nm.This colorimetric reaction is used to test for the presence of oxidation products in fats and oils, an official method for detecting them by the American Oil Chemists' Society. [9]

  7. Thioanisole - Wikipedia

    en.wikipedia.org/wiki/Thioanisole

    Thioanisole is an organic compound with the formula CH 3 SC 6 H 5.It is a colorless liquid that is soluble in organic solvents. It is the simplest alkyl–aryl thioether. The name indicates that this compound is the sulfur analogue—the thioether rather than the oxygen-centered ether—of anisole.

  8. 2,2-Dimethylbutane - Wikipedia

    en.wikipedia.org/wiki/2,2-Dimethylbutane

    Butlerov's student V. Goryainov originally discovered neohexane in 1872 by cross-coupling of zinc ethyl with tert-butyl iodide. [5]2,2-Dimethylbutane can be synthesised by the hydroisomerisation of 2,3-dimethylbutane using an acid catalyst.

  9. 6-Hydroxymelatonin - Wikipedia

    en.wikipedia.org/wiki/6-Hydroxymelatonin

    6-Hydroxymelatonin (6-OHM) is a naturally occurring, endogenous, major active metabolite of melatonin. [1] 6-Hydroxymelatonin is produced as a result of the enzymatic conversion of melatonin through hydroxylation. [2]