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  2. 3,4,5-Trimethoxybenzaldehyde - Wikipedia

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

    3,4,5-Trimethoxybenzaldehyde is an organic compound and a biochemical. Within this class of compounds, the chemical is categorized as a trisubstituted aromatic aldehyde . Uses

  3. Corey–Kim oxidation - Wikipedia

    en.wikipedia.org/wiki/Corey–Kim_oxidation

    Rather, it is formed by oxidation of dimethyl sulfide with an oxidant (NCS). The reaction mechanism of Corey–Kim oxidation. Under Corey–Kim conditions allylic and benzylic alcohols have a tendency to evolve to the corresponding allyl and benzyl chlorides unless the alcohol activation is very quickly followed by addition of triethylamine. In ...

  4. Benzamide - Wikipedia

    en.wikipedia.org/wiki/Benzamide

    Benzamide is an organic compound with the chemical formula of C 7 H 7 NO. It is the simplest amide derivative of benzoic acid. In powdered form, it appears as a white solid, while in crystalline form, it appears as colourless crystals. [5] It is slightly soluble in water, [2] and soluble in many organic solvents. [6]

  5. Benzaldehyde oxime - Wikipedia

    en.wikipedia.org/wiki/Benzaldehyde_oxime

    Benzaldehyde oxime is an organic compound with the formula C 7 H 7 NO. Benzaldehyde oxime can be synthesized from benzaldehyde and hydroxylamine hydrochloride in presence of a base. The reaction at room temperature in methanol gives 9% E -isomer and 82% Z -isomer.

  6. Hammett equation - Wikipedia

    en.wikipedia.org/wiki/Hammett_equation

    In organic chemistry, the Hammett equation describes a linear free-energy relationship relating reaction rates and equilibrium constants for many reactions involving benzoic acid derivatives with meta- and para-substituents to each other with just two parameters: a substituent constant and a reaction constant.

  7. Knorr pyrrole synthesis - Wikipedia

    en.wikipedia.org/wiki/Knorr_pyrrole_synthesis

    The Knorr pyrrole synthesis is a widely used chemical reaction that synthesizes substituted pyrroles (3). [1] [2] [3] The method involves the reaction of an α-amino-ketone (1) and a compound containing an electron-withdrawing group (e.g. an ester as shown) α to a carbonyl group (2). [4] The Knorr pyrrole synthesis

  8. 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.

  9. 3,3'-Diaminobenzidine - Wikipedia

    en.wikipedia.org/wiki/3,3'-Diaminobenzidine

    3,3′-Diaminobenzidine (DAB) is an organic compound with the formula (C 6 H 3 (NH 2) 2) 2. This derivative of benzidine is a precursor to polybenzimidazole , which forms fibers that are renowned for their chemical and thermal stability. [ 1 ]

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