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  2. Cyclopentanol - Wikipedia

    en.wikipedia.org/wiki/Cyclopentanol

    Melting point: −19 °C (−2 °F; 254 K) Boiling point: 139 to 140 °C (282 to 284 °F; 412 to 413 K) ... Cyclopentanol or cyclopentyl alcohol is a cyclic alcohol ...

  3. Amyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Amyl_alcohol

    Amyl alcohol isomers; Common name Structure Type IUPAC name Boiling point (°C) [3] 1-pentanol or normal amyl alcohol primary Pentan-1-ol: 138.5 2-methyl-1-butanol

  4. Cyclopentene - Wikipedia

    en.wikipedia.org/wiki/Cyclopentene

    Melting point: −135 °C (−211 °F; 138 K) Boiling point: 44 to 46 °C (111 to 115 °F; 317 to 319 K) ... it is prepared by dehydration of cyclopentanol. [4]

  5. Cyclopentane - Wikipedia

    en.wikipedia.org/wiki/Cyclopentane

    Its freezing point is −94 °C and its boiling point is 49 °C. Cyclopentane is in the class of cycloalkanes, being alkanes that have one or more carbon rings. It is formed by cracking cyclohexane in the presence of alumina at a high temperature and pressure. It was first prepared in 1893 by the German chemist Johannes Wislicenus. [5]

  6. Cyclopentanone - Wikipedia

    en.wikipedia.org/wiki/Cyclopentanone

    Cyclopentanone is common precursor to fragrances, especially those related to jasmine and jasmone.Examples include 2-pentyl- and 2-heptylcyclopentanone. [4] It is a versatile synthetic intermediate, being a precursor to cyclopentobarbital.

  7. 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.

  8. 3-Pentanol - Wikipedia

    en.wikipedia.org/wiki/3-Pentanol

    Melting point: −63.68 °C (−82.62 °F; 209.47 K) Boiling point: 115.3 °C (239.5 °F; 388.4 K) ... Flash point: 41 °C (106 °F; 314 K) Autoignition

  9. 1-Pentanol - Wikipedia

    en.wikipedia.org/wiki/1-Pentanol

    The hydroxyl group (OH) is the active site of many reactions. The ester formed from 1-pentanol and butyric acid is pentyl butyrate, which has an apricot-like odor.The ester formed from 1-pentanol and acetic acid is amyl acetate (also called pentyl acetate), which has a banana-like odor.