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  2. Methyl propiolate - Wikipedia

    en.wikipedia.org/wiki/Methyl_propiolate

    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.

  3. Category:Methyl esters - Wikipedia

    en.wikipedia.org/wiki/Category:Methyl_esters

    Pages in category "Methyl esters" The following 200 pages are in this category, out of approximately 303 total. ... Methyl propiolate; Methyl propionate; Methyl ...

  4. Methyl propionate - Wikipedia

    en.wikipedia.org/wiki/Methyl_propionate

    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 ]

  5. Propiolic acid - Wikipedia

    en.wikipedia.org/wiki/Propiolic_acid

    Propiolic acid is the organic compound with the formula HC 2 CO 2 H. It is the simplest acetylenic carboxylic acid. It is a colourless liquid that crystallises to give silky crystals. Near its boiling point, it decomposes. It is soluble in water and possesses an odor like that of acetic acid. [4] [5]

  6. Molar concentration - Wikipedia

    en.wikipedia.org/wiki/Molar_concentration

    To create the solution, 11.6 g NaCl is placed in a volumetric flask, dissolved in some water, then followed by the addition of more water until the total volume reaches 100 mL. The density of water is approximately 1000 g/L and its molar mass is 18.02 g/mol (or 1/18.02 = 0.055 mol/g). Therefore, the molar concentration of water is

  7. Dimethyl acetylenedicarboxylate - Wikipedia

    en.wikipedia.org/wiki/Dimethyl_acetylenedi...

    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 .

  8. Trimethylborane - Wikipedia

    en.wikipedia.org/wiki/Trimethylborane

    When trimethylborane forms an adduct with trimethylamine, steric repulsion between the methyl groups on the B and N results. The ECW model can provide a measure of this steric effect. Trimethylborane reacts with water and chlorine at room temperature. It also reacts with grease but not with teflon or glass. [5]

  9. Propyl propanoate - Wikipedia

    en.wikipedia.org/wiki/Propyl_propanoate

    Propyl propanoate (also known as propyl propionate and n-propyl propionate) is the organic compound with the molecular formula C 6 H 12 O 2. It is the ester of propanol and propionic acid. Like most esters, propyl propanoate is a colorless liquid with a fruity odor. The scent of propyl propionate is described as a chemically tinged pineapple or ...