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 552295-08-6
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
4-Chloro-6-iodothieno[2,3-d]pyrimidine features a fused thienopyrimidine core with orthogonal halogen substituents enabling selective cross-coupling. The chlorine and iodine positions facilitate sequential functionalization in transition-metal-catalyzed reactions, offering precise control over molecular architecture. This scaffold delivers high reactivity under standard conditions while maintaining bench stability.
4-Chloro-6-iodothieno[2,3-d]pyrimidine serves as a versatile building block for constructing bioactive heterocycles, enabling palladium-catalyzed cross-coupling reactions with high efficiency. The molecule’s complementary halogen functionality—chlorine at C4 and iodine at C6—facilitates sequential functionalization, while its thienopyrimidine core provides structural rigidity and favorable electronic properties for medicinal chemistry applications. Bench-stable and readily purified by crystallization, it is well-suited for scalable synthesis of kinase inhibitors and other pharmaceutical scaffolds.
|
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: