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  2. Isobutyraldehyde - Wikipedia

    en.wikipedia.org/wiki/Isobutyraldehyde

    Isobutyraldehyde is the chemical compound with the formula (CH 3) 2 CHCHO. It is an aldehyde, isomeric with n-butyraldehyde (butanal). [1] Isobutyraldehyde is made, often as a side-product, by the hydroformylation of propene. Its odour is described as that of wet cereal or straw. It undergoes the Cannizaro reaction even though it has alpha ...

  3. Butyraldehyde - Wikipedia

    en.wikipedia.org/wiki/Butyraldehyde

    Butyraldehyde undergoes reactions typical of alkyl aldehydes, and these define many of the uses of this compound.Important reactions include hydrogenation to the alcohol, oxidation to the acid, and base-catalyzed condensation.

  4. Isobutyric acid - Wikipedia

    en.wikipedia.org/wiki/Isobutyric_acid

    Isobutyric acid is manufactured by the oxidation of isobutyraldehyde, which is a byproduct of the hydroformylation of propylene. [7] It can also be prepared by the high pressure hydrocarboxylation (Koch reaction) from propylene: [7] CH 3 CH=CH 2 + CO + H 2 O → (CH 3) 2 CHCO 2 H

  5. Isobutylidenediurea - Wikipedia

    en.wikipedia.org/wiki/Isobutylidenediurea

    It is produced by the condensation reaction of isobutyraldehyde and two equivalents of urea: (CH 3) 2 CHCHO + 2 OC(NH 2) 2 → (CH 3) 2 CHCH{NHC(O)NH 2} 2 + H 2 O. The controlled-release process is the reverse of the above reaction, which only occurs after the IBDU dissolves.

  6. Isobutyryl-CoA - Wikipedia

    en.wikipedia.org/wiki/Isobutyryl-CoA

    Isobutyryl-coenzyme A is a starting material for many natural products derived from Poly-Ketide Synthase (PKS) assembly lines, as well as PKS-NRPS hybrid assembly lines. . These products can often be used as antibiot

  7. Hydroformylation - Wikipedia

    en.wikipedia.org/wiki/Hydroformylation

    Hydroformylation of an alkene (R 1 to R 3 organyl groups (i. e. alkyl-or aryl group) or hydrogen). In organic chemistry, hydroformylation, also known as oxo synthesis or oxo process, is an industrial process for the production of aldehydes (R−CH=O) from alkenes (R 2 C=CR 2).

  8. Isovaleraldehyde - Wikipedia

    en.wikipedia.org/wiki/Isovaleraldehyde

    Synthetic routes for the production of isovaleraldehyde vary. One method is by the hydroformylation of isobutene: (CH 3) 2 C=CH 2 + H 2 + CO → (CH 3) 2 C−CH 2 CHO. A small amount of 2,2-dimethylpropanal ((CH 3) 2 C−C(CHO)CH 3 side product is also generated.

  9. α-Ketoisovaleric acid - Wikipedia

    en.wikipedia.org/wiki/Α-Ketoisovaleric_acid

    α-Ketoisovaleric acid is an organic compound with the formula (CH 3) 2 CHC(O)CO 2 H. It is a ketoacid.With a melting point just above room temperature, it is usually an oil or semi-solid.