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 1300750-78-0
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2-Bromo-5-iodopyridin-4-amine delivers a dual halogenation pattern on a pyridine scaffold, enabling efficient cross-coupling strategies in medicinal chemistry. The bromo and iodo groups facilitate sequential Pd-catalyzed transformations, while the primary amine supports direct derivatization or conjugation. This bifunctional reactivity profile supports rapid diversification of heterocyclic architectures in target-oriented synthesis.
2-Bromo-5-iodopyridin-4-amine serves as a versatile building block in cross-coupling chemistry, enabling efficient access to substituted pyridine scaffolds. Its dual halogen functionality supports sequential or orthogonal coupling reactions, facilitating the construction of complex heterocyclic systems. The amine group provides additional handle for derivatization, while the compound exhibits good bench stability and compatibility with standard Pd-catalyzed transformations.
|
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-P330-P362+P364-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: