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  2. 1,3-Cyclohexanedione - Wikipedia

    en.wikipedia.org/wiki/1,3-Cyclohexanedione

    1,3-Cyclohexanedione is an organic compound with the formula (CH 2) 4 (CO) 2. It is one of three isomeric cyclohexanediones. It is a colorless compound that occurs ...

  3. Dimedone - Wikipedia

    en.wikipedia.org/wiki/Dimedone

    Dimedone is an organic compound with the formula (CH 3) 2 C(CH 2) 2 (CO) 2 (CH 2). Classified as a cyclic diketone, it is a derivative of 1,3-cyclohexanedione. It is a white solid that is soluble in water, as well as ethanol and methanol. It once was used as a reagent to test for the aldehyde functional group.

  4. Speckle tracking echocardiography - Wikipedia

    en.wikipedia.org/wiki/Speckle_Tracking...

    This method of documentation of myocardial motion is a noninvasive method of definition for both vectors and velocity. When compared to other technologies seeking noninvasive definition of ischemia, speckle tracking seems a valuable endeavor. The speckle pattern is a mixture of interference patterns and natural acoustic reflections. [1]

  5. Cyclohexa-1,3-diene - Wikipedia

    en.wikipedia.org/wiki/Cyclohexa-1,3-diene

    Cyclohexa-1,3-diene is an organic compound with the formula (C 2 H 4)(CH) 4. It is a colorless, flammable liquid. Its refractive index is 1.475 (20 °C, D).

  6. Nuclear reaction analysis - Wikipedia

    en.wikipedia.org/wiki/Nuclear_reaction_analysis

    15 N + 1 H → 12 C + α + γ (4.43 MeV) [2] with a sharp resonance in the reaction cross section at 6.385 MeV of only 1.8 keV. [3] Since the incident 15 N ion loses energy along its trajectory in the material it must have an energy higher than the resonance energy to induce the nuclear reaction with hydrogen nuclei deeper in the target.

  7. C6H8O2 - Wikipedia

    en.wikipedia.org/wiki/C6H8O2

    1,4-Cyclohexanedione; Cyclotene (maple lactone) cis-1,2-Dihydrocatechol; Methylene cyclopropyl acetic acid; 5-Methylfurfuryl alcohol; Parasorbic acid; Sorbic acid

  8. Cyclohexanedione - Wikipedia

    en.wikipedia.org/wiki/Cyclohexanedione

    1,2-Cyclohexanedione; 1,3-Cyclohexanedione; 1,4-Cyclohexanedione This page was last edited on 23 June 2017, at 01:22 (UTC). Text is available under the Creative ...

  9. Dicarbonyl - Wikipedia

    en.wikipedia.org/wiki/Dicarbonyl

    General structure of 1,2-, 1,3-, and 1,4-dicarbonyls. In organic chemistry, a dicarbonyl is a molecule containing two carbonyl (C=O) groups.Although this term could refer to any organic compound containing two carbonyl groups, it is used more specifically to describe molecules in which both carbonyls are in close enough proximity that their reactivity is changed, such as 1,2-, 1,3-, and 1,4 ...