Home Chemistry Heterocyclic Building Blocks Pyrimidines 2-Ethoxypyrimidine
Nucleophilic Substitution: The ethoxy group can undergo nucleophilic substitution reactions with certain electrophiles. For example, it can be replaced by nucleophiles such as hydroxide, amine, or thiol groups.
Alkylation or Acylation of the Pyrimidine Ring: The nitrogen atoms in the pyrimidine ring are nucleophilic and can react with alkyl halides or acyl halides in the presence of a base to form alkylated or acylated derivatives of pyrimidine.
Oxidation: Depending on the conditions, 2-ethoxypyrimidine may undergo oxidation reactions, potentially leading to the formation of products with oxidized functionalities.
Esterification: The hydroxyl group on the ethoxy moiety may undergo esterification reactions with carboxylic acids or acid chlorides, forming ester derivatives.
Reductive Reactions: The pyrimidine ring may undergo reductive reactions, such as reduction of the nitrogen atoms or the ring itself, under specific conditions.
Condensation Reactions: Depending on the reaction conditions, 2-ethoxypyrimidine may participate in condensation reactions with other compounds, forming larger structures.
N-Oxide Formation: Under certain oxidative conditions, the nitrogen atoms in the pyrimidine ring may be oxidized to form N-oxides.
Framework+−
By Key Group+−
By Parent Nucleus+−
By Functional Group+−
Heterocyclic related+−
Formula Weight+−
* Country/Region
* Quantity Required :
* Cat. No.:
* CAS No :
* Product Name :
* Additional Information :