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  2. Propyl group - Wikipedia

    en.wikipedia.org/wiki/Propyl_group

    In organic chemistry, a propyl group is a three-carbon alkyl substituent with chemical formula −CH 2 CH 2 CH 3 for the linear form. This substituent form is obtained by removing one hydrogen atom attached to the terminal carbon of propane . [ 1 ]

  3. Formate - Wikipedia

    en.wikipedia.org/wiki/Formate

    Hydrolysis of methyl formate gives formic acid and regenerates methanol: HCOOCH 3 → HCOOH + CH 3 OH. Formic acid is used for many applications in industry. Formate esters often are fragrant or have distinctive odors. Compared to the more common acetate esters, formate esters are less commonly used commercially because they are less stable. [5]

  4. List of esters - Wikipedia

    en.wikipedia.org/wiki/List_of_esters

    Structure Ethyl formate [15] Ethyl acetate [16] Ethyl propionate [17] Ethyl lactate [18] Ethyl butyrate [19] ... Structure Propyl acetate: Propyl propanoate: Propyl ...

  5. Methyl formate - Wikipedia

    en.wikipedia.org/wiki/Methyl_formate

    Methyl formate, also called methyl methanoate, is the methyl ester of formic acid. The simplest example of a carboxylate ester, it is a colorless liquid with an ethereal odour, high vapor pressure, and low surface tension. It is a precursor to many other compounds of commercial interest. [4]

  6. Alkyl group - Wikipedia

    en.wikipedia.org/wiki/Alkyl_group

    The structure of 3-methylpentane is viewed as consisting of two parts. First, five atoms comprise the longest straight chain of carbon centers. ... 2-propyl ะก 4: n ...

  7. C4H8O2 - Wikipedia

    en.wikipedia.org/wiki/C4H8O2

    Isopropyl formate Index of chemical compounds with the same molecular formula This set index page lists chemical structure articles associated with the same molecular formula .

  8. Isobutyl formate - Wikipedia

    en.wikipedia.org/wiki/Isobutyl_formate

    Isobutyl formate (2-methylpropyl methanoate) is an organic ester with the chemical formula C 5 H 10 O 2. It is formed by the Fischer esterification of isobutanol with formic acid, with the aid of an acid catalyst. It is used as a flavor and fragrance ingredient because of its odor which is sweet, ethereal, and slightly fruity. [2] [3]

  9. Methyl propionate - Wikipedia

    en.wikipedia.org/wiki/Methyl_propionate

    Condensation of Methyl propionate with formaldehyde followed by dehydration yields methyl methacrylate: [4]. MeO 2 CCH 2 CH 3 + CH 2 O → MeO 2 CCH(CH 2 OH)CH 3 MeO 2 CCH(CH 2 OH)CH 3 → MeO 2 CC(=CH 2)CH 3