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  2. Cyclooctadiene iridium methoxide dimer - Wikipedia

    en.wikipedia.org/wiki/Cyclooctadiene_iridium_m...

    Cyclooctadiene iridium methoxide dimer is an organoiridium compound with the formula Ir 2 (OCH 3) 2 (C 8 H 12) 2, where C 8 H 12 is the diene 1,5-cyclooctadiene. It is a yellow solid that is soluble in organic solvents. The complex is used as a precursor to other iridium complexes, some of which are used in homogeneous catalysis. [1]

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  4. Dimethyl ether - Wikipedia

    en.wikipedia.org/wiki/Dimethyl_ether

    As well as winning they beat the old standing record of 306 km/liter (326.8 cm 3 /100 km), set by the same team in 2007. [ 27 ] To study the dimethyl ether for the combustion process a chemical kinetic mechanism [ 28 ] is required which can be used for Computational fluid dynamics calculation.

  5. Methoxy group - Wikipedia

    en.wikipedia.org/wiki/Methoxy_group

    In nature, methoxy groups are found on nucleosides that have been subjected to 2′-O-methylation, for example in variations of the 5′-cap structure known as cap-1 and cap-2. They are also common substituents in O -methylated flavonoids , whose formation is catalyzed by O-methyltransferases that act on phenols , such as catechol- O -methyl ...

  6. 2,2-Dimethoxypropane - Wikipedia

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

    2,2-Dimethoxypropane (DMP) is an organic compound with the formula (CH 3) 2 C(OCH 3) 2.A colorless liquid, it is the product of the condensation of acetone and methanol.DMP is used as a water scavenger in water-sensitive reactions.

  7. Solubility table - Wikipedia

    en.wikipedia.org/wiki/Solubility_table

    Substance Formula 0 °C 10 °C 20 °C 30 °C 40 °C 50 °C 60 °C 70 °C 80 °C 90 °C 100 °C Barium acetate: Ba(C 2 H 3 O 2) 2: 58.8: 62: 72: 75: 78.5: 77: 75

  8. Anisole - Wikipedia

    en.wikipedia.org/wiki/Anisole

    Anisole undergoes electrophilic aromatic substitution reaction at a faster speed than benzene, which in turn reacts more quickly than nitrobenzene.The methoxy group is an ortho/para directing group, which means that electrophilic substitution preferentially occurs at these three sites.

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