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  2. Epoxide - Wikipedia

    en.wikipedia.org/wiki/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. They are produced on a large scale for many applications.

  3. Ethylene oxide - Wikipedia

    en.wikipedia.org/wiki/Ethylene_oxide

    Ethylene oxide is an organic compound with the formula C 2 H 4 O. It is a cyclic ether and the simplest epoxide: a three-membered ring consisting of one oxygen atom and two carbon atoms. Ethylene oxide is a colorless and flammable gas with a faintly sweet odor.

  4. Tetrahydrofuran - Wikipedia

    en.wikipedia.org/wiki/Tetrahydrofuran

    Tetrahydrofuran (THF), or oxolane, is an organic compound with the formula (CH 2) 4 O. The compound is classified as heterocyclic compound, specifically a cyclic ether. It is a colorless, water-miscible organic liquid with low viscosity. It is mainly used as a precursor to polymers. [8]

  5. 1,6-Hexanediol diglycidyl ether - Wikipedia

    en.wikipedia.org/.../1,6-Hexanediol_diglycidyl_ether

    1,6-Hexanediol diglycidyl ether is an organic chemical in the glycidyl ether family. It is an aliphatic compound that is a colorless liquid. It has two epoxide (oxirane) groups per molecule. Its main use is in modifying epoxy resins especially viscosity reduction whilst flexibilizing. [2] It is REACH registered. [3]

  6. Oxirene - Wikipedia

    en.wikipedia.org/wiki/Oxirene

    Oxirene is a heterocyclic chemical compound which contains an unsaturated three-membered ring containing two carbon atoms and one oxygen atom. The molecule was synthesized in low temperature ices and detected upon sublimation by isomer selective photoionization reflectron time-of-flight mass spectrometry.

  7. Tetrahydropyran - Wikipedia

    en.wikipedia.org/wiki/Tetrahydropyran

    Although tetrahydropyran is an obscure compound, tetrahydropyranyl ethers are commonly used in organic synthesis. Specifically, the 2-tetrahydropyranyl (THP) group is a common protecting group for alcohols. [5] [6] Alcohols react with 3,4-dihydropyran to give 2-tetrahydropyranyl ethers. These ethers are resilient to a variety of reactions.

  8. Crown ether - Wikipedia

    en.wikipedia.org/wiki/Crown_ether

    In organic chemistry, crown ethers are cyclic chemical compounds that consist of a ring containing several ether groups (R−O−R’). The most common crown ethers are cyclic oligomers of ethylene oxide , the repeating unit being ethyleneoxy, i.e., −CH 2 CH 2 O− .

  9. C12–C14 alcohol glycidyl ether - Wikipedia

    en.wikipedia.org/wiki/C12–C14_alcohol_glycidyl...

    C12-C14 alcohol glycidyl ether (AGE) is an organic chemical in the glycidyl ether family. [2] It is a mixture of mainly 12 and 14 carbon chain alcohols, also called fatty alcohols that have been glycidated. It is an industrial chemical used as a surfactant but primarily for epoxy resin viscosity reduction. [3]