Home Chemistry Heterocyclic Building Blocks Pyridines (5-Bromopyridin-2-Yl)Methanamine
Nucleophilic Substitution: The bromine atom can be substituted by a nucleophile in a substitution reaction. This could be a nucleophilic aromatic substitution (SNAr) where the amine group acts as a nucleophile.
Acylation: The amine group can undergo acylation reactions, where it reacts with acyl halides or acid anhydrides to form amides.
Alkylation: The amine group can be alkylated using alkyl halides or other alkylating agents.
Reductive Amination: The amine group can undergo reductive amination reactions with carbonyl compounds in the presence of reducing agents to form secondary or tertiary amines.
Oxidation: The amine group can be oxidized to form an amine oxide or further to a nitro compound or other oxidation products.
Condensation Reactions: The amine group can participate in condensation reactions with carbonyl compounds to form imines or Schiff bases.
Heterocyclic Chemistry: The molecule can participate in various heterocyclic chemistry reactions due to the presence of the pyridine ring.
Framework+−
By Key Group+−
By Parent Nucleus+−
By Functional Group+−
Heterocyclic related+−
Formula Weight+−
click to sign in and save
(5-Bromopyridin-2-yl)methanamine dihydrochloride
click to sign in and save
(5-Bromopyridin-2-yl)methanamine hydrochloride
click to sign in and save
(5-Bromo-4-methylpyridin-2-yl)methanamine hydrochloride
click to sign in and save
(5-bromo-3-methylpyridin-2-yl)methanamine hydrochloride
* Country/Region
* Quantity Required :
* Cat. No.:
* CAS No :
* Product Name :
* Additional Information :