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  2. 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 ...

  3. 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. Upon acid-catalyzed reaction, DMP reacts quantitatively with water to form acetone and methanol. [2]

  4. 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]

  5. Guaiacol - Wikipedia

    en.wikipedia.org/wiki/Guaiacol

    Guaiacol (/ ˈ ɡ w aɪ ə k ɒ l /) is an organic compound with the formula C 6 H 4 (OH)(OCH 3).It is a phenolic compound containing a methoxy functional group. Guaiacol appears as a viscous colorless oil, although aged or impure samples are often yellowish.

  6. Dimethyl ether - Wikipedia

    en.wikipedia.org/wiki/Dimethyl_ether

    Dimethyl ether (DME; also known as methoxymethane) is the organic compound with the formula CH 3 OCH 3, (sometimes ambiguously simplified to C 2 H 6 O as it is an isomer of ethanol). The simplest ether , it is a colorless gas that is a useful precursor to other organic compounds and an aerosol propellant that is currently being demonstrated for ...

  7. Methyltrichlorosilane - Wikipedia

    en.wikipedia.org/wiki/Methyltrichlorosilane

    MeSiCl 3 + 3 H 2 O → MeSi(OH) 3 + 3 HCl. The silanol is unstable and will eventually condense to give a polymer network: MeSi(OH) 3 → MeSiO 1.5 + 1.5 H 2 O. Methyltrichlorosilane undergoes alcoholysis (reaction with alcohol) to give alkoxysilanes. Methanol converts it to trimethoxymethylsilane: MeSiCl 3 + 3 CH 3 OH → MeSi(OCH 3) 3 + 3 HCl

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  9. Cyclooctadiene rhodium chloride dimer - Wikipedia

    en.wikipedia.org/wiki/Cyclooctadiene_rhodium...

    The molecule consists of a pair of square planar Rh centers bound to a 1,5-cyclooctadiene and two chloride ligands that are shared between the Rh centers. The Rh 2 Cl 2 core is also approximately planar, [4] in contrast to the highly bent structure of cyclooctadiene iridium chloride dimer where the dihedral angle is 86°.