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  2. Propylene oxide - Wikipedia

    en.wikipedia.org/wiki/Propylene_oxide

    Propylene oxide is an acutely toxic and carcinogenic organic compound with the molecular formula C 3 H 6 O. This colourless volatile liquid with an odour similar to ether, is produced on a large scale industrially.

  3. Epoxide - Wikipedia

    en.wikipedia.org/wiki/Epoxide

    A generic epoxide. In organic chemistry, an epoxide is a cyclic ether, where the ether forms a three-atom ring: two atoms of carbon and one atom of oxygen.This triangular structure has substantial ring strain, making epoxides highly reactive, more so than other ethers.

  4. Ethylene oxide - Wikipedia

    en.wikipedia.org/wiki/Ethylene_oxide

    The heterocyclic triangular structure of ethylene oxide was proposed by 1868 or earlier. [ 18 ] Wurtz's 1859 synthesis long remained the only method of preparing ethylene oxide, despite numerous attempts, including by Wurtz himself, to produce ethylene oxide directly from ethylene . [ 19 ]

  5. C3H6O - Wikipedia

    en.wikipedia.org/wiki/C3H6O

    (S)-(–)-methyl oxirane, CAS number 16088-62-3 Index of chemical compounds with the same molecular formula This set index page lists chemical structure articles associated with the same molecular formula .

  6. Oxidation with dioxiranes - Wikipedia

    en.wikipedia.org/wiki/Oxidation_with_dioxiranes

    As oxygen transfer occurs, the plane of the oxirane is perpendicular to and bisects the plane of the alkene pi system. The configuration of the alkene is maintained in the product, ruling out long-lived radical intermediates.

  7. IUPAC polymer nomenclature - Wikipedia

    en.wikipedia.org/wiki/IUPAC_polymer_nomenclature

    Polymer nomenclature usually applies to idealized representations meaning minor structural irregularities are ignored. A polymer can be named in one of two ways. Source-based nomenclature can be used when the monomer can be identified. Alternatively, more explicit structure-based nomenclature can be used when the polymer structure is proven.

  8. Trimethylolethane triglycidyl ether - Wikipedia

    en.wikipedia.org/wiki/Trimethylolethane...

    As the molecule has 3 oxirane functionalities, a key use is modifying and reducing the viscosity of epoxy resins but giving higher functionality. [7] These reactive diluent modified epoxy resins may then be further formulated into CASE applications: Coatings, Adhesives, Sealants, and Elastomers. The use of the diluent does effect mechanical ...

  9. Phenyl glycidyl ether - Wikipedia

    en.wikipedia.org/wiki/Phenyl_glycidyl_ether

    Phenyl glycidyl ether, is a liquid aromatic organic chemical in the glycidyl ether class of compounds. [2] It has the formula C 9 H 10 O 2.It has the CAS Registry Number 122-60-1 and the IUPAC name of 2-(phenoxymethyl)oxirane.