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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 .

  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. List of compounds with carbon number 8 - Wikipedia

    en.wikipedia.org/wiki/List_of_compounds_with...

    isobutyraldehyde isobutylhydrazone: 21041-71-4 C 8 H 18 O: isobutyl ether: 628-55-7 C 8 H 18 O: isooctanol: 26952-21-6 C 8 H 18 O: isopropyl pentyl ether: 5756-37-6 C 8 H 18 O: pentyl propyl ether: 18641-82-2 C 8 H 18 O 2: hexanal dimethyl acetal: 1599-47-9 C 8 H 18 O 2 S: diisobutyl sulfone: 10495-45-1 C 8 H 18 O 2 Si ...

  7. Hydroxypivaldehyde - Wikipedia

    en.wikipedia.org/wiki/Hydroxypivaldehyde

    A colorless liquid, it is produced by condensation of formaldehyde and isobutyraldehyde: [2] CH 2 O + (CH 3) 2 CHCHO → HOCH 2 (CH 3) 2 CCHO. The compound is a rare example of a distillable aldol (3-hydroxyaldehyde). Upon standing, it dimerizes reversibly to the dioxane derivative.

  8. Aldehyde - Wikipedia

    en.wikipedia.org/wiki/Aldehyde

    Aldehyde structure. In organic chemistry, an aldehyde (/ ˈ æ l d ɪ h aɪ d /) is an organic compound containing a functional group with the structure R−CH=O. [1] The functional group itself (without the "R" side chain) can be referred to as an aldehyde but can also be classified as a formyl group.

  9. C4H8O - Wikipedia

    en.wikipedia.org/wiki/C4H8O

    Isobutyraldehyde; 2-Methoxypropene; Tetrahydrofuran This page was last edited on 16 January 2019, at 11:06 (UTC). Text is available under the Creative Commons ...