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  2. Formic acid - Wikipedia

    en.wikipedia.org/wiki/Formic_acid

    Formic acid is a source for a formyl group for example in the formylation of N-methylaniline to N-methylformanilide in toluene. [20] In synthetic organic chemistry, formic acid is often used as a source of hydride ion, as in the Eschweiler–Clarke reaction: The Eschweiler–Clark reaction

  3. List of esters - Wikipedia

    en.wikipedia.org/wiki/List_of_esters

    An ester of carboxylic acid. R stands for any group (organic or inorganic) and R′ stands for organyl group. In chemistry, an ester is a compound derived from an acid (organic or inorganic) in which the hydrogen atom (H) of at least one acidic hydroxyl group (−OH) of that acid is replaced by an organyl group (−R).

  4. Ammonium formate - Wikipedia

    en.wikipedia.org/wiki/Ammonium_formate

    Formic acid can also be obtained by reacting ammonium formate with a dilute acid, and since ammonium formate is also produced from formic acid, it can serve as a way of storing formic acid. Ammonium formate can also be used in palladium on carbon (Pd/C) reduction of functional groups.

  5. Fossil preparation - Wikipedia

    en.wikipedia.org/wiki/Fossil_preparation

    An acid is applied to the surface of the rock to etch away the matrix from the surface, leaving carbonaceous tissue protruding. (Surfaces not to be etched can be coated in a wax (e.g. Vaseline or grease). This is usually accomplished by placing the rock upside-down in a weak, continually stirred acid, so that any debris can be washed away.

  6. 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]

  7. List of carboxylic acids - Wikipedia

    en.wikipedia.org/wiki/List_of_carboxylic_acids

    The systematic IUPAC name is not always the preferred IUPAC name, for example, lactic acid is a common, and also the preferred, name for what systematic rules call 2-hydroxypropanoic acid. This list is ordered by the number of carbon atoms in a carboxylic acid.

  8. Potassium formate - Wikipedia

    en.wikipedia.org/wiki/Potassium_formate

    Potassium formate, HCO 2 K, HCOOK, or KHCO 2, is the potassium salt of formic acid. This strongly hygroscopic white solid [2] is an intermediate in the formate potash process for the production of potassium. [3] Potassium formate has also been studied as a potential environmentally friendly deicing salt for use on roads.

  9. Formylation - Wikipedia

    en.wikipedia.org/wiki/Formylation

    Formylation generally involves the use of formylation agents, reagents that give rise to the CHO group. Among the many formylation reagents, particularly important are formic acid and carbon monoxide. [1] A formylation reaction in organic chemistry refers to organic reactions in which an organic compound is functionalized with a formyl group