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Benzyl benzoate is an effective and inexpensive topical treatment for human scabies. [7] It has vasodilating and spasmolytic effects and is present in many asthma and whooping cough drugs. [ 8 ] It is also used as an excipient in some testosterone -replacement medications (like Nebido ) for treating hypogonadism .
Methyl benzoate; Methyl cinnamate; Methyl dihydrojasmonate; Methyl ester of rosin, partially hydrogenated; Methyl isovalerate; Methyl linoleate (48%) Methyl linolenate (52%) mixture; Methyl naphthyl ketone; Methyl nicotinate; Methyl phenylacetate; Methyl salicylate; Methyl sulfide; 3-Methyl-1-cyclopentadecanone; 4-Methyl-1-phenyl-2-pentanone; 5 ...
In IUPAC nomenclature, the prefix benzyl refers to a C 6 H 5 CH 2 substituent, for example benzyl chloride or benzyl benzoate. Benzyl is not to be confused with phenyl with the formula C 6 H 5 . The term benzylic is used to describe the position of the first carbon bonded to a benzene or other aromatic ring.
Benzoyl peroxide is a chemical compound (specifically, an organic peroxide) with structural formula (C 6 H 5 −C(=O)O−) 2, often abbreviated as (BzO) 2.In terms of its structure, the molecule can be described as two benzoyl (C 6 H 5 −C(=O)−, Bz) groups connected by a peroxide (−O−O−).
The benzoyl functional group.. In organic chemistry, benzoyl (/ ˈ b ɛ n z oʊ ɪ l /, BENZ-oh-il) [1] is the functional group with the formula −COC 6 H 5 and structure −C(=O)−C 6 H 5. [2] [3] It can be viewed as benzaldehyde missing one hydrogen.
It can also be prepared by Friedel–Crafts acylation of benzene with benzoyl chloride in the presence of a Lewis acid (e.g. aluminium chloride) catalyst: since benzoyl chloride can itself be produced by the reaction of benzene with phosgene the first synthesis proceeded directly from those materials.
Denatonium, usually available as denatonium benzoate (under trade names such as Denatrol, BITTERANT-b, BITTER+PLUS, Bitrex, Bitrix, and Aversion) and as denatonium saccharinate (BITTERANT-s), is the most bitter chemical compound known, with bitterness thresholds of 0.05 ppm for the benzoate and 0.01 ppm for the saccharinate. [1]
The reaction produces benzyl benzoate. [4] The Tishchenko reaction: benzaldehyde reacts to benzyl benzoate, the catalyst is sodium benzylate. Enolizable aldehydes are not amenable to Claisen's conditions. Vyacheslav Tishchenko discovered that aluminium alkoxides allowed the conversion of enolizable aldehydes to esters.