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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
An ester of carboxylic acid.R stands for any group (organic or inorganic) and R′ stands for organyl group.. In chemistry, an ester is a compound derived from an acid (organic or inorganic) in which the hydrogen atom (H) of at least one acidic hydroxyl group (−OH) of that acid is replaced by an organyl group (−R).
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.
General chemical structure of a paraben (a para-hydroxybenzoate) where R = an alkyl group. Parabens are chemical compounds that are commonly used as preservatives in cosmetic and pharmaceutical products. Chemically, they are a series of parahydroxybenzoates or esters of parahydroxybenzoic acid (also known as 4-hydroxybenzoic acid). Research is ...
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.
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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 .