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  2. Diol - Wikipedia

    en.wikipedia.org/wiki/Diol

    Provided that there are enough carbon atoms that the angle strain is not too much, a cyclic ether can be formed. A common diol reaction to produce a cyclic ether. 1,2-diols and 1,3-diols can be protected using a protecting group. [13] Protecting groups are used so that the functional group does not react to future reactions.

  3. 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.

  4. Ether - Wikipedia

    en.wikipedia.org/wiki/Ether

    A cyclic ether and high-boiling solvent (b.p. 101.1 °C). Tetrahydrofuran (THF) A cyclic ether, one of the most polar simple ethers that is used as a solvent. Anisole (methoxybenzene) An aryl ether and a major constituent of the essential oil of anise seed. Crown ethers: Cyclic polyethers that are used as phase transfer catalysts. Polyethylene ...

  5. 2,2,4,4-Tetramethyl-1,3-cyclobutanediol - Wikipedia

    en.wikipedia.org/wiki/2,2,4,4-Tetramethyl-1,3-cy...

    Like BPA, CBDO is a diol with a structure suitable for making polyesters. CBDO’s C 4 ring is sufficiently rigid to prevent the two OH groups from forming cyclic structures. Unlike BPA, there is no current evidence of carcinogenic or toxic effects from CBDO-based consumer products.

  6. Protecting group - Wikipedia

    en.wikipedia.org/wiki/Protecting_group

    Orthogonal protection is a strategy allowing the specific deprotection of one protective group in a multiply-protected structure. For example, the amino acid tyrosine could be protected as a benzyl ester on the carboxyl group, a fluorenylmethylenoxy carbamate on the amine group, and a tert-butyl ether on the phenol

  7. Spiro compound - Wikipedia

    en.wikipedia.org/wiki/Spiro_compound

    Particularly common spiro compounds are ketal (acetal) formed by condensation of cyclic ketones and diols and dithiols. [15] [16] [17] A simple case is the acetal 1,4-dioxaspiro[4.5]decane from cyclohexanone and glycol. Cases of such ketals and dithioketals are common.

  8. C3H6O2 - Wikipedia

    en.wikipedia.org/wiki/C3H6O2

    4 Cyclic. Toggle Cyclic subsection. ... The molecular formula C 3 H 6 O 2 may refer to: Acids and esters ... 2-Propene-1,2-diol; Oxyethenol. 1-Methoxyethenol; Cyclic

  9. Neopentyl glycol - Wikipedia

    en.wikipedia.org/wiki/Neopentyl_glycol

    Neopentyl glycol (IUPAC name: 2,2-dimethylpropane-1,3-diol) is an organic chemical compound. It is used in the synthesis of polyesters , paints , lubricants , and plasticizers . When used in the manufacture of polyesters, it enhances the stability of the product towards heat, light, and water.