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  2. Methoxy group - Wikipedia

    en.wikipedia.org/wiki/Methoxy_group

    The structure of a typical methoxy group. In organic chemistry, a methoxy group is the functional group consisting of a methyl group bound to oxygen.This alkoxy group has the formula R−O−CH 3.

  3. 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.

  4. Solubility table - Wikipedia

    en.wikipedia.org/wiki/Solubility_table

    The tables below provides information on the variation of solubility of different substances (mostly inorganic compounds) in water with temperature, at one atmosphere pressure. Units of solubility are given in grams of substance per 100 millilitres of water (g/(100 mL)), unless shown otherwise. The substances are listed in alphabetical order.

  5. Infrared spectroscopy correlation table - Wikipedia

    en.wikipedia.org/wiki/Infrared_spectroscopy...

    N─H primary amines: any 3400–3500 strong 1560–1640 strong secondary amines any >3000 weak to medium ammonium ions any 2400–3200 multiple broad peaks C─O alcohols: primary 1040–1060 strong, broad secondary ~1100 strong tertiary 1150–1200 medium phenols any 1200 ethers aliphatic 1120 aromatic 1220–1260 carboxylic acids any 1250–1300

  6. Dimethyl carbonate - Wikipedia

    en.wikipedia.org/wiki/Dimethyl_carbonate

    Dimethyl carbonate (DMC) is an organic compound with the formula OC(OCH 3) 2.It is a colourless, flammable liquid. It is classified as a carbonate ester.This compound has found use as a methylating agent and as a co-solvent in lithium-ion batteries. [1]

  7. Trimethoxysilane - Wikipedia

    en.wikipedia.org/wiki/Trimethoxysilane

    Trimethoxysilane is an important substance for producing silane coupling agents. It contains both hydrolyzable siloxane bonds as well as an active silicon-hydrogen bond. . Thereby it can be utilized in a series of reactions, such as copolymerization, polycondensation, and disproportionation reacti

  8. Grignard reagent - Wikipedia

    en.wikipedia.org/wiki/Grignard_reagent

    Grignard reagents serve as a base for non-protic substrates (this scheme does not show workup conditions, which typically includes water). Grignard reagents are basic and react with alcohols, phenols, etc. to give alkoxides (ROMgBr). The phenoxide derivative is susceptible to formylation by paraformaldehyde to give salicylaldehyde. [18]

  9. Acetoxy group - Wikipedia

    en.wikipedia.org/wiki/Acetoxy_group

    The structure of the acetoxy group blue.. In organic chemistry, the acetoxy group (abbr. AcO or OAc; IUPAC name: acetyloxy [1]), is a functional group with the formula −OCOCH 3 and the structure −O−C(=O)−CH 3.