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 1060816-58-1
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
5-Bromo-2-chloro-7H-pyrrolo[2,3-d]pyrimidine features a fused heterocyclic core with strategically positioned halogen substituents. The electron-deficient pyrimidine ring enables direct functionalization in cross-coupling reactions. This bench-stable compound serves as a key intermediate for nucleoside analogs and kinase inhibitors.
5-Bromo-2-chloro-7H-pyrrolo[2,3-d]pyrimidine serves as a versatile building block for the synthesis of purine-based scaffolds. Its dual halogenation pattern enables sequential cross-coupling reactions with high regiocontrol, facilitating access to functionalized heterocycles used in medicinal chemistry and agrochemical development. The compound exhibits excellent bench stability and compatibility with palladium-catalyzed coupling protocols, simplifying purification and scale-up.
|
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: