Preparation of Organic Nitrates from Aryldiazoacetates and Fe(NO3)3·9H2O was written by Thurow, Samuel;Fernandes, Alessandra A. G.;Quevedo-Acosta, Yovanny;de Oliveira, Matheus F.;de Oliveira, Marcelo G.;Jurberg, Igor D.. And the article was included in Organic Letters in 2019.Recommanded Product: 6834-42-0 This article mentions the following:
A thermal protocol is reported for the formal insertion of nitric acid into aryldiazoacetates using Fe(NO3)3·9H2O. This strategy is mild and high yielding and gave a large variety of members of an unprecedented family of organic nitrates. The nitrate group can be also readily transformed into other functional groups and heterocyclic moieties and can possibly allow new biol. explorations of untapped potential associated with their NO-releasing ability. In the experiment, the researchers used many compounds, for example, 2-(3-Methoxyphenyl)acetyl chloride (cas: 6834-42-0Recommanded Product: 6834-42-0).
2-(3-Methoxyphenyl)acetyl chloride (cas: 6834-42-0) belongs to organic chlorides. Organochlorines stimulate the central nervous system and cause convulsions, tremor, nausea, and mental confusion. Examples are dichlorodiphenyltrichloroethane (DDT), chlordane, lindane, endosulfan, and dieldrin.While alkyl bromides and iodides are more reactive, alkyl chlorides tend to be less expensive and more readily available. Alkyl chlorides readily undergo attack by nucleophiles.Recommanded Product: 6834-42-0
Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics