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  2. 9-Anthracenemethanol - Wikipedia

    en.wikipedia.org/wiki/9-Anthracenemethanol

    9-Anthracenemethanol is the derivative of anthracene with a hydroxymethyl group (CH 2 OH) attached to the 9-position. It is a colorless solid that is soluble in ordinary organic solvents. The compound can be prepared by hydrogenation of 9-anthracenecarboxaldehyde. It is a versatile precursor to supramolecular assemblies. [1]

  3. Anthracene - Wikipedia

    en.wikipedia.org/wiki/Anthracene

    Anthracene is a solid polycyclic aromatic hydrocarbon (PAH) of formula C 14 H 10, consisting of three fused benzene rings. It is a component of coal tar.Anthracene is used in the production of the red dye alizarin and other dyes.

  4. Anthracene-9-carbaldehyde - Wikipedia

    en.wikipedia.org/wiki/Anthracene-9-carbaldehyde

    Anthracene-9-carbaldehyde is the most common monoaldehyde derivative of anthracene. It is a yellow solid that is soluble in common organic solvents. It is prepared by Vilsmeier formylation of anthracene. [1] [2] The compound is also used as a building block for supramolecular assemblies. [3]

  5. Morindone - Wikipedia

    en.wikipedia.org/wiki/Morindone

    1 Preparation. 2 Use as a dye. 3 References. Toggle the table of contents. Morindone. ... 1,2,5-Trihydroxy-6-methylanthracene-9,10-dione. Other names Morindone ...

  6. 9,10-Dihydroanthracene - Wikipedia

    en.wikipedia.org/wiki/9,10-Dihydroanthracene

    9,10-Dihydroanthracene is an organic compound that is derived from the polycyclic aromatic hydrocarbon anthracene. Several isomers of dihydroanthracene are known, but the 9,10 derivative is most common. It is a colourless solid that is used as a carrier of H 2 as a hydrogen-donor. [2]

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  8. Weinreb ketone synthesis - Wikipedia

    en.wikipedia.org/wiki/Weinreb_ketone_synthesis

    Weinreb and Nahm originally proposed the following reaction mechanism to explain the selectivity shown in reactions of the Weinreb–Nahm amide. Their suggestion was that the tetrahedral intermediate (A below) formed as a result of nucleophilic addition by the organometallic reagent is stabilized by chelation from the methoxy group as shown. [1]

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