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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.

  3. Tetramethyl orthosilicate - Wikipedia

    en.wikipedia.org/wiki/Tetramethyl_orthosilicate

    Tetramethyl orthosilicate (TMOS) is the chemical compound with the formula Si(OCH 3) 4.This molecule consists of four methoxy groups bonded to a silicon atom. The basic properties are similar to the more popular tetraethyl orthosilicate, which is usually preferred because the product of hydrolysis, ethanol, is less toxic than methanol.

  4. Trimethyl borate - Wikipedia

    en.wikipedia.org/wiki/Trimethyl_borate

    Trimethyl borate is the organoboron compound with the formula B(OCH 3) 3 and a metal alkoxide. It is a colourless liquid that burns with a green flame. [1] It is an intermediate in the preparation of sodium borohydride and is a popular reagent in organic chemistry.

  5. 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.

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  7. Infrared spectroscopy correlation table - Wikipedia

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

    weak to strong (usually 3 or 4) 1500 1580 1600 C≡C terminal alkynes 2100–2140 weak disubst. alkynes 2190–2260 very weak (often indistinguishable) C=O aldehyde/ketone saturated aliph./cyclic 6-membered 1720 α,β-unsaturated 1685 aromatic ketones 1685 cyclic 5-membered 1750 cyclic 4-membered 1775 aldehydes 1725

  8. 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

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