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1,3-Diols are described as syn or anti depending on the relative stereochemistries of the carbon atoms bearing the hydroxyl functional groups. Zincophorin is a natural product that contains both syn and anti 1,3-diols. Zincophorin depicting syn and anti-1,3-diol configurations
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.
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.
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
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 ...
Benzene-1,3-diol is the name recommended by the International Union of Pure and Applied Chemistry (IUPAC) in its 1993 Recommendations for the Nomenclature of Organic Chemistry. [29] Resorcinol is so named because of its derivation from ammoniated resin gum, and for its relation to the chemical orcinol. [30]
1 Non-geminal diols (glycols) 2 Geminal diols. Toggle the table of contents. ... a vicinal diol; 1,3-Propanediol, a.k.a. trimethylene glycol; Geminal diols
In organic chemistry, dihydroxybenzenes ... benzene-1,3-diol benzene-1,4-diol Other names ... All three isomers have the chemical formula C 6 H 6 O 2.