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  2. 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. [5] Cyclopentobarbital, a drug made from cyclopentanone

  3. Cyclopentenone - Wikipedia

    en.wikipedia.org/wiki/Cyclopentenone

    2-Cyclopentenones can be synthesized in a number of ways. One of the routes involves elimination of α-bromo-cyclopentanone using lithium carbonate [2] and Claisen condensation-decarboxylation-isomerization cascades of unsaturated diesters as shown below. [3] Industrial synthesis of cyclopentenone

  4. Cyclopentanol - Wikipedia

    en.wikipedia.org/wiki/Cyclopentanol

    Download as PDF; Printable version; In other projects ... Chemical formula. C 5 H 10 O: Molar mass: 86.1323 g/mol ... Cyclopentanone:

  5. C5H10 - Wikipedia

    en.wikipedia.org/wiki/C5H10

    Isomers with the molecular formula C 5 H 10 with CAS numbers. C 5 H 10 is the molecular formula of 13 hydrocarbon isomers (represented by their CAS numbers on the chart). They can be divided into cycloalkanes and alkenes.

  6. Cyclopentane - Wikipedia

    en.wikipedia.org/wiki/Cyclopentane

    Cyclopentane (also called C pentane) [4] is a highly flammable alicyclic hydrocarbon with chemical formula C 5 H 10 and CAS number 287-92-3, consisting of a ring of five carbon atoms each bonded with two hydrogen atoms above and below the plane. It is a colorless liquid with a petrol-like odor.

  7. 2-(2-(4-Methyl-3-cyclohexen-1-yl)propyl)cyclopentanone ...

    en.wikipedia.org/wiki/2-(2-(4-Methyl-3...

    The specific rotation is reported to be [α] D 20 =+228–235° (1 M; chloroform) [2] In general, the compound features a fruity apricot-like odor. Of the four stereo isomers , (2 R ,2′ S ,1′′ R )-Nectaryl and (2 R ,2′ R ,1′′ R )-Nectaryl contribute especially to the compound's odor, the odor detection threshold lies at 0.094 ng·l ...

  8. Cycloalkane - Wikipedia

    en.wikipedia.org/wiki/Cycloalkane

    Eclipsing of hydrogen atoms is an important destabilizing effect, as well. The strain energy of a cycloalkane is the increase in energy caused by the compound's geometry, and is calculated by comparing the experimental standard enthalpy change of combustion of the cycloalkane with the value calculated using average bond energies. Molecular ...

  9. Hansen solubility parameter - Wikipedia

    en.wikipedia.org/wiki/Hansen_solubility_parameter

    Hansen solubility parameters were developed by Charles M. Hansen in his Ph.D thesis in 1967 [1] [2] as a way of predicting if one material will dissolve in another and form a solution. [3] They are based on the idea that like dissolves like where one molecule is defined as being 'like' another if it bonds to itself in a similar way.

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