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  2. Diol - Wikipedia

    en.wikipedia.org/wiki/Diol

    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. Benzylidene groups are used to protect 1,3-diols. [13]

  3. 1,3-Propanediol - Wikipedia

    en.wikipedia.org/wiki/1,3-Propanediol

    1,3-Propanediol is the organic compound with the formula CH 2 (CH 2 OH) 2. This 3-carbon diol is a colorless viscous liquid that is miscible with water. Products

  4. Alkanediol - Wikipedia

    en.wikipedia.org/wiki/Alkanediol

    Example of a 1,2-diol (Ethyleneglycol, top),a 1,3-diol (1,3-Propanediol, middle)and a 1,4-diol (1,4-Butanediol, bottom).An alkanediol, composed of alkane and diol, are a group of substances consisting of linear or branched hydrocarbon chains containing exactly two hydroxy groups at different positions.

  5. 1,3-Butanediol - Wikipedia

    en.wikipedia.org/wiki/1,3-Butanediol

    1,3-Butanediol is an organic compound with the formula CH 3 CH(OH)CH 2 CH 2 OH, not to be confused with 1,4 Butanediol. With two alcohol functional groups, the molecule is classified as a diol . The compound without the R (or D) designation is racemic, which is what has been used in most studies before 2023.

  6. Acetonide - Wikipedia

    en.wikipedia.org/wiki/Acetonide

    General structure of a 1,2-acetonide. The diol is shown in blue, the acetone part in red. In organic chemistry, an acetonide is the functional group composed of the cyclic ketal of a diol with acetone. The more systematic name for this structure is an isopropylidene ketal. Acetonide is a common protecting group for 1,2- and 1,3-diols. [1]

  7. Butanediol - Wikipedia

    en.wikipedia.org/wiki/Butanediol

    2-methylpropane-1,2-diol; 2-methylpropane-1,3-diol; and one unstable geminal diol: 2-methylpropane-1,1-diol (not a glycol), hydrate of 2-methylpropanal (isobutyraldehyde) These three methylpropanediols are structural isomers of butanediols. They are not chiral.

  8. Methylbenzenediol - Wikipedia

    en.wikipedia.org/wiki/Methylbenzenediol

    Orcinol (5-methylbenzene-1,3-diol or 3,5-dihydroxytoluene) 2-methylbenzene-1,4-diol; See also. Cresol (methylphenol, hydroxytoluene) Trihydroxytoluene

  9. Dihydroxybenzenes - Wikipedia

    en.wikipedia.org/wiki/Dihydroxybenzenes

    4-Methylcatechol (4-methylbenzene-1,2-diol) Orcinol (5-methylbenzene-1,3-diol) Methoxyphenols — can be derived from benzenediols by O-methylation. Guaiacol (2-methoxyphenol, O-Methylcatechol) Mequinol (4-Methoxyphenol) Dimethoxybenzenes — can be derived from benzenediols by two rounds of O-methylation. Veratrole (1,2-Dimethoxybenzene) 1,3 ...