Synthesis of some new 4-(3H)-quinazoline analogs as potential antioxidant agents was written by Al-Omar, M. A.;El-Azab, Adel E.;El-Obeid, H. A.;Abdel Hamide, S. G.. And the article was included in Journal of Saudi Chemical Society in 2006.Recommanded Product: 2-Amino-4-iodobenzoic acid This article mentions the following:
A new series of derivatives of 6-iodo-2-propyl-4(3H)-quinazolinone [I, R = H] and its fused heterocyclic analogs were prepared and screened for their antioxidant activity. I [R = H, NHCONH2, OH, phthalimido, NH2, O2CCH2Cl,OCH2CONH2] inhibit aldehyde oxidase exclusively by more than 98 %. This type of inhibition was found to be competitive with Ki value ranging from 50-400 μM with respect to aldehyde oxidase. In the experiment, the researchers used many compounds, for example, 2-Amino-4-iodobenzoic acid (cas: 20776-54-9Recommanded Product: 2-Amino-4-iodobenzoic acid).
2-Amino-4-iodobenzoic acid (cas: 20776-54-9) belongs to iodide derivatives. Typical reactions of alkyl iodides include nucleophilic substitution, elimination, reduction, and the formation of organometallics. In the chemical industry, alkyl iodides serve as excellent alkylating agents and, specifically, methyl iodide is used as a methylating agent in the synthesis of various pharmaceutical drugs.Recommanded Product: 2-Amino-4-iodobenzoic acid
Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com