Home Chemistry Heterocyclic Building Blocks Pyridines 6-Methylpyridin-2-Amine
Nucleophilic substitution: The amine group can undergo substitution reactions with electrophiles. For example, it can react with alkyl halides to form N-alkylated products.
Acylation: The amine group can react with acyl chlorides or acid anhydrides to form amides. This reaction typically requires a base catalyst.
Alkylation: The pyridine ring can undergo alkylation reactions with alkyl halides or alkylating agents under appropriate conditions.
Redox reactions: The compound can participate in redox reactions, either as a reducing agent or as an oxidizing agent depending on the reaction conditions.
Condensation reactions: It can participate in condensation reactions, particularly with carbonyl compounds, to form imines or Schiff bases.
Substitution reactions on the pyridine ring: Depending on the reaction conditions and the nature of the substituents, various substitution reactions such as halogenation, nitration, and sulfonation can occur.
Metal complex formation: The amine nitrogen can coordinate with transition metals to form metal complexes, which may exhibit catalytic or other interesting properties.
Framework+−
By Key Group+−
By Parent Nucleus+−
By Functional Group+−
Heterocyclic related+−
Formula Weight+−
click to sign in and save
5-Bromo-3-methoxy-6-methylpyridin-2-amine
click to sign in and save
6-Methyl-5-(trifluoromethyl)pyridin-2-amine
click to sign in and save
5-(Difluoromethoxy)-6-methylpyridin-2-amine
click to sign in and save
N-(6-Amino-2-methylpyridin-3-yl)acetamide
* Country/Region
* Quantity Required :
* Cat. No.:
* CAS No :
* Product Name :
* Additional Information :