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  2. 1, 2, 3, 4 (Sumpin' New) - Wikipedia

    en.wikipedia.org/wiki/1,_2,_3,_4_(Sumpin'_New)

    Larry Flick from Billboard described the song as "a jumpy, funk-lined jeep anthem that allows Coolio plenty of room to work up a fun, lyrical sweat."He added, "The sample-happy groove provides a wigglin' good time, riding primarily on a prominent snippet of the early '80s 12-incher "Wikka Wrap" by the Evasions.

  3. 1, 2, 3, 4 (Plain White T's song) - Wikipedia

    en.wikipedia.org/wiki/1,_2,_3,_4_(Plain_White_T's...

    The music video for the song premiered on the MySpace main page January 16, 2009 and was subsequently released on MTV, MTVU, VH1, Fuse, Music Choice and YouTube. It found success on the weekly VH1 Top 20 Video Countdown, charting over five months straight between January and May, peaking at #5.

  4. 1 + 2 + 3 + 4 + ⋯ - Wikipedia

    en.wikipedia.org/wiki/1_%2B_2_%2B_3_%2B_4_%2B_%E...

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us; Donate; Pages for logged out editors learn more

  5. 1,2,4-Trichlorobenzene - Wikipedia

    en.wikipedia.org/wiki/1,2,4-Trichlorobenzene

    The LD50 (oral, rats) is 756 mg/kg. Animal studies have shown that 1,2,4-trichlorobenzene affects the liver and kidney, and is possibly a teratogen. There is no regulated occupational exposure limit for chemical exposure, but the National Institute for Occupational Safety and Health recommends no greater exposure than 5 ppm, over an 8-hour workday.

  6. 1,2,4-Triazole - Wikipedia

    en.wikipedia.org/wiki/1,2,4-Triazole

    1,2,4-Triazole (as ligand in coordination compounds, Htrz abbreviation is sometimes used) is one of a pair of isomeric chemical compounds with molecular formula C 2 H 3 N 3, called triazoles, which have a five-membered ring of two carbon atoms and three nitrogen atoms. 1,2,4-Triazole and its derivatives find use in a wide variety of ...

  7. 1,2,3,4-Tetraphenylnaphthalene - Wikipedia

    en.wikipedia.org/wiki/1,2,3,4-Tetraphenylnaphthalene

    Infobox references. 1,2,3,4-Tetraphenylnaphthalene is a polycyclic aromatic hydrocarbon commonly prepared in the undergraduate teaching laboratory as an introduction to the Diels-Alder reaction, in this case between benzyne, which acts as the dienophile, (generated in situ) and tetraphenylcyclopentadienone, which acts as the diene. [3]

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