Nucleophilicities of selected ions in water at 195 °C was written by Reed, Gregg A.;Dimmel, Donald R.;Malcolm, Earl W.. And the article was included in Journal of Organic Chemistry in 1993.Recommanded Product: 6515-58-8 This article mentions the following:
The reaction of a benzyl aryl ether with selected ions was studied to determine relative nucleophilicities at 195 °C in water. Nucleophilic displacement by the ions occurred at the benzyl carbon to liberate a phenolic group. The primary products of the displacement were independently synthesized and reacted in alkali to determine their stability. Hydrosulfide ion was 20 times more reactive than hydroxide ion with this substrate, while anthrahydroquinone ion was 17 times more reactive. In the experiment, the researchers used many compounds, for example, 3-(Bromomethyl)benzoic acid (cas: 6515-58-8Recommanded Product: 6515-58-8).
3-(Bromomethyl)benzoic acid (cas: 6515-58-8) belongs to organobromine compounds. Organo bromine compounds are versatile compounds and are widely used in diverse fields. Organo bromine derivatives are used in the dye sector, as an indicator in analytical chemistry (Bromothymol blue is a popular indicator). The reactivity of organobromine compounds resembles but is intermediate between the reactivity of organochlorine and organoiodine compounds. For many applications, organobromides represent a compromise of reactivity and cost.Recommanded Product: 6515-58-8
Referemce:
Bromide – Wikipedia,
bromide – Wiktionary