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  2. 2,5-Furandicarboxylic acid - Wikipedia

    en.wikipedia.org/wiki/2,5-Furandicarboxylic_acid

    2,5-Furandicarboxylic acid (FDCA) is an organic chemical compound consisting of two carboxylic acid groups attached to a central furan ring. It was first reported as dehydromucic acid by Rudolph Fittig and Heinzelmann in 1876, who produced it via the action of concentrated hydrobromic acid upon mucic acid . [ 2 ]

  3. 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.

  4. Dicarboxylic acid - Wikipedia

    en.wikipedia.org/wiki/Dicarboxylic_acid

    In organic chemistry, a dicarboxylic acid is an organic compound containing two carboxyl groups (−COOH). The general molecular formula for dicarboxylic acids can be written as HO 2 C−R−CO 2 H, where R can be aliphatic or aromatic. In general, dicarboxylic acids show similar chemical behavior and reactivity to monocarboxylic acids.

  5. Furan fatty acids - Wikipedia

    en.wikipedia.org/wiki/Furan_fatty_acids

    Furan fatty acids in animals are based on the uptake and accumulation of furan fatty acids from plant constituents. [6] In human blood, the total furan fatty acid content is about 50 ng/ml. Per day, a person separates between 0.5 and 3 mg of urofuran acids - the metabolic product of the furans acids.

  6. Polyethylene furan-2,5-dicarboxylate - Wikipedia

    en.wikipedia.org/wiki/Polyethylene_furan-2,5-di...

    [2] [3] As an aromatic polyester from ethylene glycol it is a chemical analogue of polyethylene terephthalate (PET) and polyethylene naphthalate (PEN). PEF has been described in (patent) literature since 1951, [ 4 ] but has gained renewed attention since the US department of energy proclaimed its building block, FDCA, as a potential bio-based ...

  7. Furan - Wikipedia

    en.wikipedia.org/wiki/Furan

    Like enol ethers, 2,5-disubstituted furans are susceptible to hydrolysis to reversibly give 1,4-diketones. Furan serves as a diene in Diels–Alder reactions with electron-deficient dienophiles such as ethyl (E)-3-nitroacrylate. [15] The reaction product is a mixture of isomers with preference for the endo isomer:

  8. Perfluoroalkyl carboxylic acids - Wikipedia

    en.wikipedia.org/.../Perfluoroalkyl_carboxylic_acids

    Trifluoroacetic acid is a widely employed acid, used for example in the synthesis of peptides.Its esters are useful in analytical chemistry. Longer-chain perfluoroalkyl carboxylic acids, e.g. with five to nine carbons, are useful fluorosurfactants and emulsifiers used in the production of polytetrafluoroethylene (Teflon) and related fluoropolymers.

  9. 2,5-Dimethylfuran - Wikipedia

    en.wikipedia.org/wiki/2,5-Dimethylfuran

    2,5-Dimethylfuran is a heterocyclic compound with the formula (CH 3) 2 C 4 H 2 O. Although often abbreviated DMF , it should not be confused with dimethylformamide . A derivative of furan , this simple compound is a potential biofuel , being derivable from cellulose.