Home Chemistry Heterocyclic Building Blocks Pyrimidines 2,4-Dimethylpyrimidine
Substitution Reactions: The methyl groups on the pyrimidine ring can be subject to substitution reactions. For example, the methyl groups can be replaced by other functional groups through nucleophilic substitution or electrophilic substitution reactions.
Nucleophilic Addition: The nitrogen atoms in the pyrimidine ring can act as nucleophiles and participate in nucleophilic addition reactions. For instance, they may react with electrophiles, such as alkyl halides or acyl chlorides, to form substituted pyrimidine derivatives.
Oxidation Reactions: The nitrogen atoms in the pyrimidine ring can be oxidized under certain conditions, leading to the formation of different functional groups.
Alkylation Reactions: The pyrimidine ring can undergo alkylation reactions, where alkyl groups are introduced onto the nitrogen atoms or other positions in the ring.
Acylation Reactions: The nitrogen atoms can react with acylating agents to form amide derivatives.
Condensation Reactions: 2,4-Dimethylpyrimidine may participate in condensation reactions with other compounds, leading to the formation of larger, more complex molecules.
Reduction Reactions: The pyrimidine ring may undergo reduction reactions under certain conditions, leading to the formation of saturated derivatives.
Metalation Reactions: The pyrimidine ring can be deprotonated by strong bases, leading to the formation of metalated intermediates. These metalated species can then react with various electrophiles.
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2,4-Dimethyl-pyrimidine-5-carboxylic acid
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