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  2. File:Propan-1-ol.svg - Wikipedia

    en.wikipedia.org/wiki/File:Propan-1-ol.svg

    Date/Time Thumbnail Dimensions User Comment; current: 21:07, 2 June 2014: 244 × 64 (7 KB): Arrowsmaster: scaled up and changed the OH alignment: 16:18, 5 January 2011

  3. 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.

  4. Allyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Allyl_alcohol

    Allyl alcohol (IUPAC name: prop-2-en-1-ol) is an organic compound with the structural formula CH 2 =CHCH 2 OH. Like many alcohols, it is a water-soluble, colourless liquid. It is more toxic than typical small alcohols. Allyl alcohol is used as a precursor to many specialized compounds such as flame-resistant materials, drying oils, and ...

  5. 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

  6. 1-Propanol (data page) - Wikipedia

    en.wikipedia.org/wiki/1-Propanol_(data_page)

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  7. Propargyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Propargyl_alcohol

    Propargyl alcohol, or 2-propyn-1-ol, is an organic compound with the formula C 3 H 4 O. It is the simplest stable alcohol containing an alkyne functional group. [ 3 ] Propargyl alcohol is a colorless viscous liquid that is miscible with water and most polar organic solvents.

  8. Propylamine - Wikipedia

    en.wikipedia.org/wiki/Propylamine

    Propylamine, also known as n-propylamine, is an amine with the chemical formula CH 3 (CH 2) 2 NH 2. [1] It is a colorless volatile liquid. [2] Propylamine is a weak base. Its K b (base dissociation constant) is 4.7 × 10 −4.

  9. Propane-1,3-dithiol - Wikipedia

    en.wikipedia.org/wiki/Propane-1,3-dithiol

    Structure of (C 3 H 6 S 2) 2, the oxidized "dimer" of 1,3-propanedithiol. [4] 1,3-Propanedithiol is used in the synthesis of tiapamil. 1,3-Propanedithiol reacts with metal ions to form dithiolates. Illustrative is the synthesis of the derivative diiron propanedithiolate hexacarbonyl upon reaction with triiron dodecacarbonyl: [5] Fe 3 (CO) 12 ...