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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.
Methyl 4-iodobenzoate, or methyl p-iodobenzoate, is an organic compound with the formula IC 6 H 4 COOCH 3. [3] It is the methyl ester of 4-iodobenzoic acid , or may also be viewed as an iodinated derivative of methyl benzoate .
[me 3 o] + [bf 4] − + h 2 o → me 2 o + meoh + h + [bf 4] − Trimethyloxonium tetrafluoroborate is generally ranked as the strongest commercially available reagent for electrophilic methylation , [ 1 ] being stronger than methyl sulfonate esters, including methyl triflate and methyl fluorosulfonate ("magic methyl"). [ 2 ]
Methyl 4-bromophenylacetate is made from 4-bromophenylacetic acid by Fischer esterification, refluxing it with methanol acidified with sulfuric acid. [3] An ethyl ester can be made in an analogous way using ethanol instead of methanol. [4] A hydrazone derivative, 2-(4-bromophenyl)acetohydrazide, is made by refluxing the methyl ester with ...
tert-Butyl peroxybenzoate (TBPB) an organic compound with the formula C 6 H 5 CO 3 CMe 3 (Me = CH 3).It is the most widely produced perester; it is an ester of peroxybenzoic acid (C 6 H 5 CO 3 H).
4-Trifluoromethylbenzaldehyde is the organofluorine compound with the formula CF 3 C 6 H 4 CHO. Two other isomers are also known: 2-trifluoromethylbenzaldehyde and 3-trifluoromethylbenzaldehyde. These compounds are derivatives of benzaldehyde with trifluoromethyl substituents.
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.
R)-2-Methyl-CBS-oxazaborolidine is an organoboron catalyst that is used in organic synthesis. This catalyst , developed by Itsuno [ 1 ] [ 2 ] and Elias James Corey , [ 3 ] [ 4 ] [ 5 ] is generated by heating ( R )-(+)-2-(diphenylhydroxymethyl) pyrrolidine along with trimethylboroxine or methylboronic acid .