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  2. Propanol - Wikipedia

    en.wikipedia.org/wiki/Propanol

    Propanal (propionaldehyde) differs in spelling from propanol by a single letter and is a different compound. Propranolol is a drug used for reducing blood pressure and hand tremors. Index of chemical compounds with the same name

  3. Structural isomer - Wikipedia

    en.wikipedia.org/wiki/Structural_isomer

    Functional isomers are structural isomers which have different functional groups, resulting in significantly different chemical and physical properties. [ 11 ] An example is the pair propanal H 3 C–CH 2 –C(=O)-H and acetone H 3 C–C(=O)–CH 3 : the first has a –C(=O)H functional group, which makes it an aldehyde , whereas the second has ...

  4. Cyclopropanol - Wikipedia

    en.wikipedia.org/wiki/Cyclopropanol

    The compound is highly unstable due to the three-membered ring, and is susceptible to reactions that open the ring. It is highly prone to rearrangement, undergoing structural isomerization to form propanal. [3] [4] This property is useful synthetically: cyclopropanol can be used as a synthon for the homoenolate of propanal.

  5. 1-Propanol - Wikipedia

    en.wikipedia.org/wiki/1-Propanol

    1-Propanol (also propan-1-ol, propanol, n-propyl alcohol) is a primary alcohol with the formula CH 3 CH 2 CH 2 OH and sometimes represented as PrOH or n-PrOH.It is a colourless liquid and an isomer of 2-propanol. 1-Propanol is used as a solvent in the pharmaceutical industry, mainly for resins and cellulose esters, and, sometimes, as a disinfecting agent.

  6. Isopropyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Isopropyl_alcohol

    Isopropyl alcohol (IUPAC name propan-2-ol and also called isopropanol or 2-propanol) is a colorless, flammable, organic compound with a pungent alcoholic odor. [9]Isopropyl alcohol, an organic polar molecule, is miscible in water, ethanol, and chloroform, demonstrating its ability to dissolve a wide range of substances including ethyl cellulose, polyvinyl butyral, oils, alkaloids, and natural ...

  7. Propionaldehyde - Wikipedia

    en.wikipedia.org/wiki/Propionaldehyde

    Propionaldehyde exhibits the reactions characteristic of alkyl aldehydes, e.g. hydrogenation, aldol condensations, oxidations, etc. It is the simplest aldehyde with a prochiral methylene such that α-functionalized derivatives (CH 3 CH(X)CHO) are chiral. If water is available, propionaldehyde exists in equilibrium with 1,1-propanediol, a ...

  8. Propylene - Wikipedia

    en.wikipedia.org/wiki/Propylene

    Propylene and benzene are converted to acetone and phenol via the cumene process. Overview of the cumene process. Propylene is also used to produce isopropyl alcohol (propan-2-ol), acrylonitrile, propylene oxide, and epichlorohydrin. [18] The industrial production of acrylic acid involves the catalytic partial oxidation of propylene. [19]

  9. C3H6O - Wikipedia

    en.wikipedia.org/wiki/C3H6O

    propanal or propionaldehyde, CH 3 CH 2-CHO, CAS number 123-38-6; Ketones. Propanone or acetone, CH 3-CO-CH 3, CAS number 67-64-1; Enols (tautomers of aldehydes and ...