Lot numbers can be found on the outside label of a product:
Please log in for operation!
*For research and further manufacturing use only, not for direct human use.
Structure of 173999-23-0
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
5-Bromo-2-pyridinemethanamine features a brominated pyridine core paired with a primary amine handle, enabling direct functionalization in transition metal-catalyzed couplings. This bench-stable derivative integrates readily into bioactive scaffolds and pharmaceutical intermediates, where the electron-deficient pyridine ring enhances reactivity in nucleophilic substitution processes.
5-Bromo-2-pyridinemethanamine serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its bromine substituent. The primary amine functionality facilitates direct derivatization or incorporation into peptide-like scaffolds. Its stability under standard bench conditions and compatibility with common protecting groups make it suitable for multi-step synthesis of heterocyclic drug candidates.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302-H315-H319-H335
|
|
|
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: