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  2. 4-tert-Butylbenzaldehyde - Wikipedia

    en.wikipedia.org/wiki/4-tert-butylbenzaldehyde

    4-tert-Butylbenzaldehyde is notable as a rare example of industrial-scale electrochemistry. It is produced by BASF and Givaudan (typically as its methanol acetal) through a double anodic oxidation of 4-tert-butyltoluene on greater than 10,000 ton per year scale. [2] [3]

  3. List of water-miscible solvents - Wikipedia

    en.wikipedia.org/wiki/List_of_water-miscible...

    CH 3 CHO: acetaldehyde: 75-07-0 CH 3 CO 2 H: ... (CH 3) 2 SO: dimethyl sulfoxide: 67-68-5 C 4 H 8 O 2: 1,4-Dioxane: 123-91-1 C 2 H 6 O: ... CH 3 N(C 2 H 4 OH) 2:

  4. Azeotrope tables - Wikipedia

    en.wikipedia.org/wiki/Azeotrope_tables

    This page contains tables of azeotrope data for various binary and ternary mixtures of solvents. The data include the composition of a mixture by weight (in binary azeotropes, when only one fraction is given, it is the fraction of the second component), the boiling point (b.p.) of a component, the boiling point of a mixture, and the specific gravity of the mixture.

  5. Benzaldehyde - Wikipedia

    en.wikipedia.org/wiki/Benzaldehyde

    Amygdalin 2 H 2 O HCN benzaldehyde 2 × glucose 2 × Benzaldehyde contributes to the scent of oyster mushrooms (Pleurotus ostreatus). Reactions Benzaldehyde is easily oxidized to benzoic acid in air at room temperature, causing a common impurity in laboratory samples. Since the boiling point of benzoic acid is much higher than that of benzaldehyde, it may be purified by distillation. Benzyl ...

  6. Category:Benzaldehydes - Wikipedia

    en.wikipedia.org/wiki/Category:Benzaldehydes

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us; Pages for logged out editors learn more

  7. Leuckart reaction - Wikipedia

    en.wikipedia.org/wiki/Leuckart_reaction

    The Leuckart reaction is the chemical reaction that converts aldehydes or ketones to amines.The reaction is an example of reductive amination. [1] The reaction, named after Rudolf Leuckart, uses either ammonium formate or formamide as the nitrogen donor and reducing agent.

  8. Category:Tert-butyl compounds - Wikipedia

    en.wikipedia.org/wiki/Category:Tert-butyl_compounds

    4-tert-Butylbenzaldehyde; N-tert-Butylbenzenesulfinimidoyl chloride; Para-tert-Butylbenzoic acid; 4-tert-Butylcatechol; Tert-Butyldiphenylsilyl; Tert-Butylhydroquinone; Tert-Butyllithium; Tert-Butyloxycarbonyl protecting group; Tert-Butylphosphaacetylene; Tert-Butylthiol; N-t-Butyltryptamine; Butyrolactol A

  9. Acetaldehyde - Wikipedia

    en.wikipedia.org/wiki/Acetaldehyde

    Conversion of acetaldehyde to 1,1-diethoxyethane, R 1 = CH 3 R 2 = CH 3 CH 2 Acetaldehyde forms a stable acetal upon reaction with ethanol under conditions that favor dehydration. The product, CH 3 CH(OCH 2 CH 3 ) 2 , is formally named 1,1-diethoxyethane but is commonly referred to as "acetal". [ 39 ]