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  2. Ethylene glycol - Wikipedia

    en.wikipedia.org/wiki/Ethylene_glycol

    Ethylene glycol (IUPAC name: ethane-1,2-diol) is an organic compound (a vicinal diol [7]) with the formula (CH 2 OH) 2. It is mainly used for two purposes: as a raw material in the manufacture of polyester fibers and for antifreeze formulations. It is an odorless, colorless, flammable, viscous liquid.

  3. Diol - Wikipedia

    en.wikipedia.org/wiki/Diol

    A diol is a chemical compound containing two hydroxyl groups (−OH groups). [1] An aliphatic diol may also be called a glycol. [2] This pairing of functional groups is pervasive, and many subcategories have been identified. They are used as protecting groups of carbonyl groups, making them essential in synthesis of organic chemistry. [3]

  4. Ethane-1,2-dithiol - Wikipedia

    en.wikipedia.org/wiki/Ethane-1,2-dithiol

    Ethane-1,2-dithiol, also known as EDT, [1] is a colorless liquid with the formula C 2 H 4 2. It has a very characteristic odor which is compared by many people to rotten cabbage . It is a common building block in organic synthesis and an excellent ligand for metal ions.

  5. File:2,2,2-trichloroethane-1,1-diol 200.svg - Wikipedia

    en.wikipedia.org/wiki/File:2,2,2-trichloroethane...

    This structural formula was created with Name2Struct - CS ChemDraw Ultra. The chemistry symbols of this structural formula are drawn using the path text method. The accuracy of this version of the structural formula has been verified as part of the Chemical Structure Validation project .

  6. NanoPutian - Wikipedia

    en.wikipedia.org/wiki/Nanoputian

    Formylation of this structure was then achieved through using the organolithium reagent n-butyllithium followed by quenching with N,N-dimethylformamide (DMF) to create the aldehyde. 1,2-Ethanediol was added to this structure to protect the aldehyde using p-toluenesulfonic acid as a catalyst. Originally, Chanteau and Tour aimed to couple this ...

  7. Alcohol (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Alcohol_(chemistry)

    When necessary, the position of the hydroxyl group is indicated by a number between the alkane name and the -ol: propan-1-ol for CH 3 CH 2 CH 2 OH, propan-2-ol for CH 3 CH(OH)CH 3. If a higher priority group is present (such as an aldehyde , ketone , or carboxylic acid ), then the prefix hydroxy- is used, [ 19 ] e.g., as in 1-hydroxy-2 ...

  8. C8H10O2 - Wikipedia

    en.wikipedia.org/wiki/C8H10O2

    The molecular formula C 8 H 10 O 2 (molar mass: 138.164 g/mol) may refer to: ... 1-phenyl-1,2-ethanediol This page was last edited on 7 July 2018, at 13:10 ...

  9. 1,2-Butanediol - Wikipedia

    en.wikipedia.org/wiki/1,2-Butanediol

    1,2-Butanediol is a byproduct of the production of 1,4-butanediol from butadiene. [8] It is also a byproduct of the catalytic hydrocracking of starches and sugars such as sorbitol to ethylene glycol and propylene glycol. [9] It can also be obtained from the dihydroxylation of but-1-ene by OsO 4.