Extended knowledge of 2,2-Diphenylacetic acid

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law. In my other articles, you can also check out more blogs about 117-34-0. Quality Control of 2,2-Diphenylacetic acid.

Enzymes are biological catalysts that produce large increases in reaction rates and tend to be specific for certain reactants and products. 117-34-0, Name is 2,2-Diphenylacetic acid, molecular formula is C14H12O2, belongs to phthalazines compound. In a document, author is Zinczenko, Wiktoria, introduce the new discover, Quality Control of 2,2-Diphenylacetic acid.

Azines and Azoloazines, Part 1: Reactions of Triazolo[3,4-a]phthalazine and Its Derivatives with Carbanions

Triazolo[3,4-a]phthalazine as well as their chloro and nitro derivatives were subjected to the reactions with the carbanions typical for the vicarious nucleophilic substitution (VNS) of hydrogen. The reactions were strongly dependent on the substituents present on the triazolo[3,4-a]phthalazine ring and resulted not only in the substitution of hydrogen but also in exchange of chlorine atom and pyridazine ring scission; the latter process dominated for the unsubstituted triazolophthalazine. Two of the products showed promising stimulating activity towards the central nervous system with no significant toxic effects.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law. In my other articles, you can also check out more blogs about 117-34-0. Quality Control of 2,2-Diphenylacetic acid.

Reference:
Phthalazine – Wikipedia,
,Phthalazine | C8H6N2 – PubChem