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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 benzoate is an organic compound. It is an ester with the chemical formula C 6 H 5 COOCH 3, sometimes abbreviated as PhCO 2 Me, where Ph and Me are phenyl and methyl, respectively. Its structure is C 6 H 5 −C(=O)−O−CH 3. It is a colorless liquid that is poorly soluble in water, but miscible with organic solvents.
The complete removal of the water is critical for the reaction conversion, due to the pronounced hygroscopy of potassium hydroxide, which contains about 10% of water. [3] The significantly higher dissolution rate of potassium hydroxide in methanol compared to sodium hydroxide is advantageous.
Potassium benzoate (E212), the potassium salt of benzoic acid, is a food preservative that inhibits the growth of mold, yeast and some bacteria. It works best in low- pH products, below 4.5, where it exists as benzoic acid.
4-Bromobenzaldehyde, or p-bromobenzaldehyde, is an organobromine compound with the formula BrC 6 H 4 CHO. It is one of three isomers of bromobenzaldehyde . [ 3 ] It displays reactivity characteristic of benzaldehyde and an aryl bromide .
These solutions are identified by CAS number 75-59-2. Several hydrates such as N(CH 3) 4 OH·xH 2 O. have been crystallized. [3] These salts contain well separated Me 4 N + cations and hydroxide anions (Me is an abbreviation of methyl group). The hydroxide groups are linked by hydrogen bonds to the water of crystallization. Anhydrous TMAH has ...
One variant of the reaction involves iminodiacetonitrile or iminodiacetic acid (step 1'), which reacts in a weakly acidic medium (pH 6) with hydrogen cyanide and ethanal to form methylglycinonitrile-N,N-diacetic acid, the nitrile group of which is hydrolyzed with sodium hydroxide to trisodium N-(1-carboxylatoethyl)iminodiacetate (step 2').
GBL is known to be used in the synthesis of 4-chlorobutyryl chloride. [23] This in turn is used in the synthesis of the butyrophenone sidechain of many antipsychotic drugs (e.g. haloperidol). It is also known to be employed in the synthesis of 1-bromo-4,4-bis(p-fluorophenyl)butane [57668-61-8] [24] (the side-chain to the diphenylbutylpiperidine ...