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  2. Organoboron chemistry - Wikipedia

    en.wikipedia.org/wiki/Organoboron_chemistry

    The most-studied class of organoboron compounds has the formula BR n H 3−n. These compounds are catalysts, reagents, and synthetic intermediates. The trialkyl and triaryl derivatives feature a trigonal-planar boron center that is typically only weakly Lewis acidic. Except a few bulky derivatives, the hydrides (n = 1 or 2) dimerize, like ...

  3. Bis(pinacolato)diboron - Wikipedia

    en.wikipedia.org/wiki/Bis(pinacolato)diboron

    The B-B bond adds across alkenes and alkynes to give the 1,2-diborylated alkanes and alkenes. Using various organorhodium or organoiridium catalysts, it can also be installed onto saturated hydrocarbons: [3] CH 3 (CH 2) 6 CH 3 + [pinB] 2 → pinBH + CH 3 (CH 2) 7 Bpin. These reactions proceed via boryl complexes. Bis(pinacolato)diboron can also ...

  4. Dimethylbenzylamine - Wikipedia

    en.wikipedia.org/wiki/Dimethylbenzylamine

    Dimethylbenzylamine is the organic compound with the formula C 6 H 5 CH 2 N(CH 3) 2. The molecule consists of a benzyl group, C 6 H 5 CH 2, attached to a dimethylamino functional group. It is a colorless liquid. It is used as a catalyst for the formation of polyurethane foams and epoxy resins.

  5. Benzhydryl compounds - Wikipedia

    en.wikipedia.org/wiki/Benzhydryl_compounds

    Ball-and-stick model of diphenylmethane. The benzhydryl compounds are a group of organic compounds whose parent structures include diphenylmethane (which is two benzene rings connected by a single methane), with any number of attached substituents, including bridges.

  6. Phenylboronic acid - Wikipedia

    en.wikipedia.org/wiki/Phenylboronic_acid

    Phenylboronic acid or benzeneboronic acid, abbreviated as PhB(OH) 2 where Ph is the phenyl group C 6 H 5 - and B(OH) 2 is a boronic acid containing a phenyl substituent and two hydroxyl groups attached to boron.

  7. Ammonium benzoate - Wikipedia

    en.wikipedia.org/wiki/Ammonium_benzoate

    1.26 g/cm 3: Melting point: 198 °C (388 °F; 471 K) ... (SDS) Fisher Scientific ... Ammonium benzoate can be dehydrated to form benzamide.

  8. Diphenylmethane - Wikipedia

    en.wikipedia.org/wiki/Diphenylmethane

    The methylene group in diphenylmethane is mildly acidic with a pK a of 32.2, and so can be deprotonated with sodium amide. [3] (C 6 H 5) 2 CH 2 + NaNH 2 − → (C 6 H 5) 2 CHNa + NH 3. The resulting carbanion can be alkylated. For example, treatment with n-bromobutane produces 1,1-diphenylpentane in 92% yield. [4]

  9. 3,4,5-Trimethoxybenzaldehyde - Wikipedia

    en.wikipedia.org/wiki/3,4,5-Trimethoxybenzaldehyde

    3,4,5-Trimethoxybenzaldehyde can be used as an intermediate in the synthesis of some pharmaceutical drugs including trimethoprim, [1] [2] cintriamide, roletamide, trimethoquinol (aka tretoquinol), and trimazosin as well as some psychedelic phenethylamines.

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