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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 .
The following other wikis use this file: Usage on azb.wikipedia.org متل بنزوات; Usage on bs.wikipedia.org Ester; Usage on el.wikipedia.org
Name Structure Methyl nitrate [4] Methyl formate [5] Methyl acetate [6] Methyl acrylate: Methyl propionate [7] Methyl butyrate [8] Methyl pentanoate [9] Methyl benzoate [10] Methyl anthranilate [11] Methyl salicylate [12] Methyl phenylacetate [13] Methyl cinnamate [14]
Benzoate plasticizers, such as the glycol-, diethyleneglycol-, and triethyleneglycol esters, are obtained by transesterification of methyl benzoate with the corresponding diol. [22] These plasticizers, which are used similarly to those derived from terephthalic acid ester, represent alternatives to phthalates .
The structures of many reagents are often misunderstood because simplified formulas are presented in reaction schemes whereas the actual structures are more complex. Examples are methyl lithium and lithium diisopropylamide. Readers of Wikipedia often comment (complain) that structures shown are incorrect for this reason.
The term "methyl" was derived in about 1840 by back-formation from "methylene", and was then applied to describe "methyl alcohol". This was shortened to "methanol" in 1892 by the International Conference on Chemical Nomenclature. [29] The suffix-yl, which, in organic chemistry, forms names of carbon groups, is from the word methyl.
Benzyl group and derivatives: Benzyl group, benzyl radical, benzyl amine, benzyl bromide, benzyl chloroformate, and benzyl methyl ether. R = heteroatom, alkyl, aryl, allyl etc. or other substituents. In organic chemistry, benzyl is the substituent or molecular fragment possessing the structure R−CH 2 −C 6 H 5.
For example, the sodium benzoate is an ionic compound with the structure C 6 H 5 –CO–O − Na +, and its condensed structural formula usually written as C 6 H 5 CO 2 Na. The suffix comes from "-oic acid". The most common examples of compounds named with the "oate" suffix are esters, like ethyl acetate, CH 3 COOCH 2 CH 3.