Home Chemistry Heterocyclic Building Blocks Pyridines Thiazolo[5,4-C]Pyridine
Nucleophilic Substitution Reactions: The nitrogen and sulfur atoms in the ring can serve as nucleophiles and participate in substitution reactions. For example, they might react with electrophiles to replace a substituent.
Acylation and Alkylation Reactions: The nitrogen and sulfur atoms can act as nucleophiles in acylation and alkylation reactions, where they can react with acyl or alkyl halides, respectively.
Metal Complexation Reactions: Thiazole rings can coordinate with transition metal ions, forming complexes. This might result in changes in the reactivity of the compound.
Ring Opening Reactions: Depending on the reaction conditions and the substituents on the ring, thiazolo[5,4-c]pyridine might undergo ring-opening reactions, potentially leading to the formation of acyclic products.
Condensation Reactions: Thiazolo[5,4-c]pyridine may undergo condensation reactions with suitable reagents to form larger, more complex molecules.
Photochemical Reactions: Depending on the specific substituents and conditions, thiazolo[5,4-c]pyridine might undergo photochemical reactions when exposed to light.
Functional Group Transformations: Various functional groups, such as amino, hydroxyl, carbonyl, etc., present in thiazolo[5,4-c]pyridine may participate in a variety of reactions, including reactions that modify or transform those groups.
Framework+−
By Key Group+−
By Parent Nucleus+−
By Functional Group+−
Heterocyclic related+−
Formula Weight+−
click to sign in and save
2-Bromo-7-chlorothiazolo[5,4-c]pyridine
* Country/Region
* Quantity Required :
* Cat. No.:
* CAS No :
* Product Name :
* Additional Information :