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  2. Furan - Wikipedia

    en.wikipedia.org/wiki/Furan

    Melting point: −85.6 °C (−122.1 °F; 187.6 K) ... Furan is a colorless, flammable, highly volatile liquid with a boiling point close to room temperature.

  3. Melting points of the elements (data page) - Wikipedia

    en.wikipedia.org/wiki/Melting_points_of_the...

    The Gmelin rare earths handbook lists 1522 °C and 1550 °C as two melting points given in the literature, the most recent reference [Handbook on the chemistry and physics of rare earths, vol.12 (1989)] is given with 1529 °C.

  4. Furan resin - Wikipedia

    en.wikipedia.org/wiki/Furan_resin

    Furan resin refers to polymers produced from various furan compounds, [1] ... or at higher temperatures by adding latent curing agents such as ammonium nitrate. [4] ...

  5. Furfural - Wikipedia

    en.wikipedia.org/wiki/Furfural

    Furfural is used to make other furan derivatives, such as furoic acid, via oxidation, [30] and furan itself via palladium catalyzed vapor phase decarbonylation. [ 4 ] There is a good market for value added chemicals that can be obtained from furfural.

  6. Tammann and Hüttig temperatures - Wikipedia

    en.wikipedia.org/wiki/Tammann_and_Hüttig...

    The Tammann temperature is important for reactive compounds like explosives and fuel oxiders, such as potassium chlorate (KClO 3, T Tammann = 42 °C), potassium nitrate (KNO 3, T Tammann = 31 °C), and sodium nitrate (NaNO 3, T Tammann = 17 °C), which may unexpectedly react at much lower temperatures than their melting or decomposition ...

  7. 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]

  8. Thiophene - Wikipedia

    en.wikipedia.org/wiki/Thiophene

    At room temperature, thiophene is a colorless liquid with a mildly pleasant odor reminiscent of benzene, [citation needed] with which thiophene shares some similarities. The high reactivity of thiophene toward sulfonation is the basis for the separation of thiophene from benzene, which are difficult to separate by distillation due to their ...

  9. Furfuryl alcohol - Wikipedia

    en.wikipedia.org/wiki/Furfuryl_alcohol

    Furfuryl alcohol is an organic compound containing a furan substituted with a hydroxymethyl group. It is a colorless liquid, but aged samples appear amber. It possesses a faint odor of burning and a bitter taste. It is miscible with but unstable in water. It is soluble in common organic solvents. [4]