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  2. Neopentylamine - Wikipedia

    en.wikipedia.org/wiki/Neopentylamine

    Neopentylamine is an organic compound with the molecular formula (CH 3) 3 CCH 2 NH 2. It is a colorless liquid. The molecule is the primary amine derivative of neopentane, (CH 3) 4 C. Like most alkyl amines, it degrades slowly in air. [1]

  3. Jmol - Wikipedia

    en.wikipedia.org/wiki/Jmol

    JSmol is also free and open source under the same license. Molecules can be displayed in different styles of rendering, like ball-and-stick models , space-filling models , ribbon diagrams , etc. [ 6 ] Jmol supports a wide range of chemical file formats , including Protein Data Bank (pdb), Crystallographic Information File (cif), MDL Molfile ...

  4. Neopentyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Neopentyl_alcohol

    Neopentyl alcohol is a compound with formula (CH 3) 3 CCH 2 OH. It is a colorless solid. It is a colorless solid. The compound is one of the eight isomers of pentyl alcohol .

  5. n-Butylbenzene - Wikipedia

    en.wikipedia.org/wiki/N-Butylbenzene

    n-Butylbenzene is the organic compound with the formula C 6 H 5 C 4 H 9.Of two isomers of butylbenzene, n-butylbenzene consists of a phenyl group attached to the 1 position of a butyl group.

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  7. Neophyl chloride - Wikipedia

    en.wikipedia.org/wiki/Neophyl_chloride

    c 6 h 5 c(ch 3) 2 ch 2 oh + socl 2 → c 6 h 5 c(ch 3) 2 ch 2 cl + hcl + so 2 It is easily prepared on a large scale from benzene and methallyl chloride by an electrophilic aromatic substitution reaction, using sulfuric acid as the catalyst : [ 4 ] The reaction is an example of an electrophilic aromatic substitution reaction.

  8. 4B-MAR - Wikipedia

    en.wikipedia.org/wiki/4B-MAR

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us; Help; Learn to edit; Community portal; Recent changes; Upload file

  9. U46619 - Wikipedia

    en.wikipedia.org/wiki/U46619

    U46619 is a stable synthetic analog of the endoperoxide prostaglandin PGH 2 first prepared in 1975, [1] and acts as a thromboxane A 2 (TP) receptor agonist. It potently stimulates TP receptor-mediated, but not other prostaglandin receptor-mediated responses in various in vitro preparations and exhibits many properties similar to thromboxane A 2, including shape change and aggregation of ...