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  2. Formamide - Wikipedia

    en.wikipedia.org/wiki/Formamide

    Formamide is an amide derived from formic acid.It is a colorless liquid which is miscible with water and has an ammonia-like odor.It is chemical feedstock for the manufacture of sulfa drugs and other pharmaceuticals, herbicides and pesticides, and in the manufacture of hydrocyanic acid.

  3. Formamide-based prebiotic chemistry - Wikipedia

    en.wikipedia.org/wiki/Formamide-based_prebiotic...

    [43] [44] As well as phosphorylation, formamide has been shown to be a competent medium for the production of amino acid derivatives from their simple aldehyde and nitrile precursors, demonstrating that water is not the only solvent that this process can occur in. [45] Most notably, formamide provides a medium for the prebiotic synthesis of ...

  4. Proto-metabolism - Wikipedia

    en.wikipedia.org/wiki/Proto-metabolism

    Overall, formamide chemistry can support connections and substrates needed to support prebiotic biomolecule synthesis including the formose reaction, Strecker synthesis, HCN oligomerization, or the Fischer-Tropsch process. [11] [35] In addition, formamide can be easily concentrated through evaporation reactions as it has a boiling point of 210C.

  5. Dimethylformamide - Wikipedia

    en.wikipedia.org/wiki/Dimethylformamide

    Dimethylformamide, DMF is an organic compound with the chemical formula H C O N(CH 3) 2.Its structure is HC(=O)−N(−CH 3) 2.Commonly abbreviated as DMF (although this initialism is sometimes used for dimethylfuran, or dimethyl fumarate), this colourless liquid is miscible with water and the majority of organic liquids.

  6. Ritter reaction - Wikipedia

    en.wikipedia.org/wiki/Ritter_reaction

    A large scale application of the Ritter reaction is in the synthesis of tert-octylamine, by way of the intermediate formamide.This process was originally described by Ritter in 1948, [11] and an estimated 10,000 tons/y (year: 2000) of this and related lipophilic amines are prepared in this way. [12]

  7. Leuckart reaction - Wikipedia

    en.wikipedia.org/wiki/Leuckart_reaction

    The reaction, named after Rudolf Leuckart, uses either ammonium formate or formamide as the nitrogen donor and reducing agent. It requires high temperatures, usually between 120 and 130 °C; for the formamide variant, the temperature can be greater than 165 °C. The ketone is converted to an amine via reductive amination using ammonium formate

  8. Are Seed Oils Really Unhealthy? Dietitians Explain. - AOL

    www.aol.com/seed-oils-really-unhealthy...

    It's more difficult to get oil out of a seed than it is, say, an olive, so seeds undergo a more intense oil extraction process. People often assume that means the oils are chemical heavy—and ...

  9. Amide - Wikipedia

    en.wikipedia.org/wiki/Amide

    The core −C(=O)−(N) of amides is called the amide group (specifically, carboxamide group).. In the usual nomenclature, one adds the term "amide" to the stem of the parent acid's name.