Search results
Results from the WOW.Com Content Network
1,3-Butanediol is an organic compound with the formula CH 3 CH(OH)CH 2 CH 2 OH. With two alcohol functional groups, the molecule is classified as a diol. The compound is also chiral, but most studies do not distinguish the enantiomers. The compound is a colorless, bittersweet, water-soluble liquid. It is one of four common structural isomers of ...
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
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.
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.
Dithiothreitol (DTT) is an organosulfur compound with the formula (CH(OH)CH 2 SH) 2. A colorless compound, it is classified as a dithiol and a diol. DTT is redox reagent also known as Cleland's reagent, after W. Wallace Cleland. [2] The reagent is commonly used in its racemic form. Its name derives from the four-carbon sugar, threose.
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
All three isomers have the chemical formula C 6 H 6 O 2. ... Orcinol (5-methylbenzene-1,3-diol) Methoxyphenols — can be derived from benzenediols by O-methylation.
2,2,4,4-Tetramethyl-1,3-cyclobutanediol (CBDO) is an aliphatic diol. This diol is produced as a mixture of cis - and trans - isomers , depending on the relative stereochemistry of the hydroxyl groups.