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Methyl propiolate is an organic compound with the formula HC 2 CO 2 CH 3. It is the methyl ester of propiolic acid , the simplest acetylenic carboxylic acid . It is a colorless liquid that is miscible with organic solvents.
Pages in category "Methyl esters" The following 200 pages are in this category, out of approximately 303 total. ... Methyl propiolate; Methyl propionate; Methyl ...
This page contains tables of azeotrope data for various binary and ternary mixtures of solvents. The data include the composition of a mixture by weight (in binary azeotropes, when only one fraction is given, it is the fraction of the second component), the boiling point (b.p.) of a component, the boiling point of a mixture, and the specific gravity of the mixture.
The molecular formula C 4 H 4 O 2 may refer to: Cyclobutanediones. ... Methyl propiolate; Tetrolic acid This page was last edited on 1 October 2024, at 00:31 ...
The tables below provides information on the variation of solubility of different substances (mostly inorganic compounds) in water with temperature, at one atmosphere pressure. Units of solubility are given in grams of substance per 100 millilitres of water (g/(100 mL)), unless shown otherwise. The substances are listed in alphabetical order.
The following chart shows the solubility of various ionic compounds in water at 1 atm pressure and room temperature (approx. 25 °C, 298.15 K). "Soluble" means the ionic compound doesn't precipitate, while "slightly soluble" and "insoluble" mean that a solid will precipitate; "slightly soluble" compounds like calcium sulfate may require heat to precipitate.
Methyl propionate, also known as methyl propanoate, is an organic compound with the molecular formula CH 3 CH 2 CO 2 CH 3. It is a colorless liquid with a fruity, rum -like odor. [ 2 ]
Dimethyl acetylenedicarboxylate (DMAD) is an organic compound with the formula CH 3 O 2 CC 2 CO 2 CH 3. It is a di- ester in which the ester groups are conjugated with a C-C triple bond. As such, the molecule is highly electrophilic , and is widely employed as a dienophile in cycloaddition reactions, such as the Diels-Alder reaction .